SNP Links for Protein (Select 4885243) - SNP - NCBI

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Links from Protein

Items: 1 to 20 of 270

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Select item 14888804811.

rs1488880481 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:65893078 (GRCh38)
11:65660549 (GRCh37)
Canonical SPDI:: NC_000011.10:65893077:A:T
Gene:: FOSL1 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,3_prime_UTR_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.65893078A>T, NC_000011.9:g.65660549A>T, NG_047103.1:g.462T>A, NM_005438.5:c.624T>A, NM_005438.4:c.624T>A, NM_005438.3:c.624T>A, NM_001300855.2:c.*211T>A, NM_001300855.1:c.*211T>A, NM_001300844.2:c.516T>A, NM_001300844.1:c.516T>A, NR_125339.2:n.482T>A, NR_125339.1:n.463T>A, NM_001300856.2:c.426T>A, NM_001300856.1:c.426T>A, NM_001300857.2:c.318T>A, NM_001300857.1:c.318T>A

Select item 14793391122.

rs1479339112 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:65896964 (GRCh38)
11:65664435 (GRCh37)
Canonical SPDI:: NC_000011.10:65896963:G:C
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65896964G>C, NC_000011.9:g.65664435G>C, NM_005438.5:c.142C>G, NM_005438.4:c.142C>G, NM_005438.3:c.142C>G, NM_001300855.2:c.142C>G, NM_001300855.1:c.142C>G, NM_001300844.2:c.142C>G, NM_001300844.1:c.142C>G, NP_005429.1:p.Gln48Glu, NP_001287784.1:p.Gln48Glu, NP_001287773.1:p.Gln48Glu

Select item 14791616843.

rs1479161684 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:65900309 (GRCh38)
11:65667780 (GRCh37)
Canonical SPDI:: NC_000011.10:65900308:T:C
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.65900309T>C, NC_000011.9:g.65667780T>C, NM_005438.5:c.31A>G, NM_005438.4:c.31A>G, NM_005438.3:c.31A>G, NM_001300855.2:c.31A>G, NM_001300855.1:c.31A>G, NM_001300844.2:c.31A>G, NM_001300844.1:c.31A>G, NM_001300856.2:c.31A>G, NM_001300856.1:c.31A>G, NM_001300857.2:c.31A>G, NM_001300857.1:c.31A>G, NP_005429.1:p.Ser11Gly, NP_001287784.1:p.Ser11Gly, NP_001287773.1:p.Ser11Gly, NP_001287785.1:p.Ser11Gly, NP_001287786.1:p.Ser11Gly

Select item 14730488834.

rs1473048883 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTGTGGGGGG>- [Show Flanks]
Chromosome:: 11:65896875 (GRCh38)
11:65664346 (GRCh37)
Canonical SPDI:: NC_000011.10:65896870:GGGGTTGTGGGGGG:GGGG
Gene:: FOSL1 (Varview)
Functional Consequence:: frameshift_variant,intron_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.65896875_65896884del, NC_000011.9:g.65664346_65664355del, NM_005438.5:c.226_235del, NM_005438.4:c.226_235del, NM_005438.3:c.226_235del, NM_001300855.2:c.226_235del, NM_001300855.1:c.226_235del, NM_001300844.2:c.226_235del, NM_001300844.1:c.226_235del, NP_005429.1:p.Pro76fs, NP_001287784.1:p.Pro76fs, NP_001287773.1:p.Pro76fs

Select item 14729864205.

rs1472986420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:65893256 (GRCh38)
11:65660727 (GRCh37)
Canonical SPDI:: NC_000011.10:65893255:C:T
Gene:: FOSL1 (Varview)
Functional Consequence:: 3_prime_UTR_variant,coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.65893256C>T, NC_000011.9:g.65660727C>T, NG_047103.1:g.284G>A, NM_005438.5:c.446G>A, NM_005438.4:c.446G>A, NM_005438.3:c.446G>A, NM_001300855.2:c.*33G>A, NM_001300855.1:c.*33G>A, NM_001300844.2:c.338G>A, NM_001300844.1:c.338G>A, NR_125339.2:n.304G>A, NR_125339.1:n.285G>A, NM_001300856.2:c.248G>A, NM_001300856.1:c.248G>A, NM_001300857.2:c.140G>A, NM_001300857.1:c.140G>A, NP_005429.1:p.Arg149Gln, NP_001287773.1:p.Arg113Gln, NP_001287785.1:p.Arg83Gln, NP_001287786.1:p.Arg47Gln

Select item 14680329986.

rs1468032998 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:65896883 (GRCh38)
11:65664354 (GRCh37)
Canonical SPDI:: NC_000011.10:65896882:G:C
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.65896883G>C, NC_000011.9:g.65664354G>C, NM_005438.5:c.223C>G, NM_005438.4:c.223C>G, NM_005438.3:c.223C>G, NM_001300855.2:c.223C>G, NM_001300855.1:c.223C>G, NM_001300844.2:c.223C>G, NM_001300844.1:c.223C>G, NP_005429.1:p.Pro75Ala, NP_001287784.1:p.Pro75Ala, NP_001287773.1:p.Pro75Ala

Select item 14602389177.

rs1460238917 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:65896860 (GRCh38)
11:65664331 (GRCh37)
Canonical SPDI:: NC_000011.10:65896859:G:A,NC_000011.10:65896859:G:C
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65896860G>A, NC_000011.10:g.65896860G>C, NC_000011.9:g.65664331G>A, NC_000011.9:g.65664331G>C, NM_005438.5:c.246C>T, NM_005438.5:c.246C>G, NM_005438.4:c.246C>T, NM_005438.4:c.246C>G, NM_005438.3:c.246C>T, NM_005438.3:c.246C>G, NM_001300855.2:c.246C>T, NM_001300855.2:c.246C>G, NM_001300855.1:c.246C>T, NM_001300855.1:c.246C>G, NM_001300844.2:c.246C>T, NM_001300844.2:c.246C>G, NM_001300844.1:c.246C>T, NM_001300844.1:c.246C>G

Select item 14579610748.

rs1457961074 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:65896990 (GRCh38)
11:65664461 (GRCh37)
Canonical SPDI:: NC_000011.10:65896989:G:C
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000113/5 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000012/3 (GnomAD_exomes)
C=0.000036/5 (GnomAD)
HGVS:: NC_000011.10:g.65896990G>C, NC_000011.9:g.65664461G>C, NM_005438.5:c.116C>G, NM_005438.4:c.116C>G, NM_005438.3:c.116C>G, NM_001300855.2:c.116C>G, NM_001300855.1:c.116C>G, NM_001300844.2:c.116C>G, NM_001300844.1:c.116C>G, NP_005429.1:p.Pro39Arg, NP_001287784.1:p.Pro39Arg, NP_001287773.1:p.Pro39Arg

Select item 14573638429.

rs1457363842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:65894109 (GRCh38)
11:65661580 (GRCh37)
Canonical SPDI:: NC_000011.10:65894108:C:T
Gene:: FOSL1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65894109C>T, NC_000011.9:g.65661580C>T, NM_005438.5:c.310G>A, NM_005438.4:c.310G>A, NM_005438.3:c.310G>A, NM_001300855.2:c.305G>A, NM_001300855.1:c.305G>A, NR_125339.2:n.168G>A, NR_125339.1:n.149G>A, NM_001300856.2:c.112G>A, NM_001300856.1:c.112G>A, NP_005429.1:p.Glu104Lys, NP_001287784.1:p.Gly102Glu, NP_001287785.1:p.Glu38Lys

Select item 145610912410.

rs1456109124 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:65894041 (GRCh38)
11:65661512 (GRCh37)
Canonical SPDI:: NC_000011.10:65894040:C:T
Gene:: FOSL1 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65894041C>T, NC_000011.9:g.65661512C>T, NM_005438.5:c.378G>A, NM_005438.4:c.378G>A, NM_005438.3:c.378G>A, NM_001300855.2:c.373G>A, NM_001300855.1:c.373G>A, NR_125339.2:n.236G>A, NR_125339.1:n.217G>A, NM_001300856.2:c.180G>A, NM_001300856.1:c.180G>A, NP_001287784.1:p.Glu125Lys

Select item 145575593811.

rs1455755938 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 11:65896886 (GRCh38)
11:65664357 (GRCh37)
Canonical SPDI:: NC_000011.10:65896885:T:
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65896886del, NC_000011.9:g.65664357del, NM_005438.5:c.220del, NM_005438.4:c.220del, NM_005438.3:c.220del, NM_001300855.2:c.220del, NM_001300855.1:c.220del, NM_001300844.2:c.220del, NM_001300844.1:c.220del, NP_005429.1:p.Ser74fs, NP_001287784.1:p.Ser74fs, NP_001287773.1:p.Ser74fs

Select item 145279765012.

rs1452797650 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:65896836 (GRCh38)
11:65664307 (GRCh37)
Canonical SPDI:: NC_000011.10:65896835:T:C,NC_000011.10:65896835:T:G
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65896836T>C, NC_000011.10:g.65896836T>G, NC_000011.9:g.65664307T>C, NC_000011.9:g.65664307T>G, NM_005438.5:c.270A>G, NM_005438.5:c.270A>C, NM_005438.4:c.270A>G, NM_005438.4:c.270A>C, NM_005438.3:c.270A>G, NM_005438.3:c.270A>C, NM_001300855.2:c.270A>G, NM_001300855.2:c.270A>C, NM_001300855.1:c.270A>G, NM_001300855.1:c.270A>C, NM_001300844.2:c.270A>G, NM_001300844.2:c.270A>C, NM_001300844.1:c.270A>G, NM_001300844.1:c.270A>C

Select item 144853944013.

rs1448539440 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:65900302 (GRCh38)
11:65667773 (GRCh37)
Canonical SPDI:: NC_000011.10:65900301:C:A
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.65900302C>A, NC_000011.9:g.65667773C>A, NM_005438.5:c.38G>T, NM_005438.4:c.38G>T, NM_005438.3:c.38G>T, NM_001300855.2:c.38G>T, NM_001300855.1:c.38G>T, NM_001300844.2:c.38G>T, NM_001300844.1:c.38G>T, NM_001300856.2:c.38G>T, NM_001300856.1:c.38G>T, NM_001300857.2:c.38G>T, NM_001300857.1:c.38G>T, NP_005429.1:p.Gly13Val, NP_001287784.1:p.Gly13Val, NP_001287773.1:p.Gly13Val, NP_001287785.1:p.Gly13Val, NP_001287786.1:p.Gly13Val

Select item 144846566914.

rs1448465669 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:65893018 (GRCh38)
11:65660489 (GRCh37)
Canonical SPDI:: NC_000011.10:65893017:A:C
Gene:: FOSL1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.65893018A>C, NC_000011.9:g.65660489A>C, NG_047103.1:g.522T>G, NM_005438.5:c.684T>G, NM_005438.4:c.684T>G, NM_005438.3:c.684T>G, NM_001300855.2:c.*271T>G, NM_001300855.1:c.*271T>G, NM_001300844.2:c.576T>G, NM_001300844.1:c.576T>G, NR_125339.2:n.542T>G, NR_125339.1:n.523T>G, NM_001300856.2:c.486T>G, NM_001300856.1:c.486T>G, NM_001300857.2:c.378T>G, NM_001300857.1:c.378T>G

Select item 144835668115.

rs1448356681 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:65896904 (GRCh38)
11:65664375 (GRCh37)
Canonical SPDI:: NC_000011.10:65896903:G:A
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000085/3 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.65896904G>A, NC_000011.9:g.65664375G>A, NM_005438.5:c.202C>T, NM_005438.4:c.202C>T, NM_005438.3:c.202C>T, NM_001300855.2:c.202C>T, NM_001300855.1:c.202C>T, NM_001300844.2:c.202C>T, NM_001300844.1:c.202C>T

Select item 144589118816.

rs1445891188 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:65892918 (GRCh38)
11:65660389 (GRCh37)
Canonical SPDI:: NC_000011.10:65892917:G:T
Gene:: FOSL1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00003/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.65892918G>T, NC_000011.9:g.65660389G>T, NG_047103.1:g.622C>A, NM_005438.5:c.784C>A, NM_005438.4:c.784C>A, NM_005438.3:c.784C>A, NM_001300855.2:c.*371C>A, NM_001300855.1:c.*371C>A, NM_001300844.2:c.676C>A, NM_001300844.1:c.676C>A, NR_125339.2:n.642C>A, NR_125339.1:n.623C>A, NM_001300856.2:c.586C>A, NM_001300856.1:c.586C>A, NM_001300857.2:c.478C>A, NM_001300857.1:c.478C>A, NP_005429.1:p.Pro262Thr, NP_001287773.1:p.Pro226Thr, NP_001287785.1:p.Pro196Thr, NP_001287786.1:p.Pro160Thr

Select item 144347482417.

rs1443474824 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:65900321 (GRCh38)
11:65667792 (GRCh37)
Canonical SPDI:: NC_000011.10:65900320:CCCC:CCC
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,frameshift_variant
HGVS:: NC_000011.10:g.65900324del, NC_000011.9:g.65667795del, NM_005438.5:c.19del, NM_005438.4:c.19del, NM_005438.3:c.19del, NM_001300855.2:c.19del, NM_001300855.1:c.19del, NM_001300844.2:c.19del, NM_001300844.1:c.19del, NM_001300856.2:c.19del, NM_001300856.1:c.19del, NM_001300857.2:c.19del, NM_001300857.1:c.19del, NP_005429.1:p.Glu7fs, NP_001287784.1:p.Glu7fs, NP_001287773.1:p.Glu7fs, NP_001287785.1:p.Glu7fs, NP_001287786.1:p.Glu7fs

Select item 143858164718.

rs1438581647 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:65894063 (GRCh38)
11:65661534 (GRCh37)
Canonical SPDI:: NC_000011.10:65894062:G:A
Gene:: FOSL1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,non_coding_transcript_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.65894063G>A, NC_000011.9:g.65661534G>A, NM_005438.5:c.356C>T, NM_005438.4:c.356C>T, NM_005438.3:c.356C>T, NM_001300855.2:c.351C>T, NM_001300855.1:c.351C>T, NR_125339.2:n.214C>T, NR_125339.1:n.195C>T, NM_001300856.2:c.158C>T, NM_001300856.1:c.158C>T, NP_005429.1:p.Ala119Val, NP_001287785.1:p.Ala53Val

Select item 143658241419.

rs1436582414 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:65893100 (GRCh38)
11:65660571 (GRCh37)
Canonical SPDI:: NC_000011.10:65893099:C:A,NC_000011.10:65893099:C:G
Gene:: FOSL1 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000113/4 (ALFA)
G=0.000029/4 (GnomAD)
G=0.000045/12 (TOPMED)
HGVS:: NC_000011.10:g.65893100C>A, NC_000011.10:g.65893100C>G, NC_000011.9:g.65660571C>A, NC_000011.9:g.65660571C>G, NG_047103.1:g.440G>T, NG_047103.1:g.440G>C, NM_005438.5:c.602G>T, NM_005438.5:c.602G>C, NM_005438.4:c.602G>T, NM_005438.4:c.602G>C, NM_005438.3:c.602G>T, NM_005438.3:c.602G>C, NM_001300855.2:c.*189G>T, NM_001300855.2:c.*189G>C, NM_001300855.1:c.*189G>T, NM_001300855.1:c.*189G>C, NM_001300844.2:c.494G>T, NM_001300844.2:c.494G>C, NM_001300844.1:c.494G>T, NM_001300844.1:c.494G>C, NR_125339.2:n.460G>T, NR_125339.2:n.460G>C, NR_125339.1:n.441G>T, NR_125339.1:n.441G>C, NM_001300856.2:c.404G>T, NM_001300856.2:c.404G>C, NM_001300856.1:c.404G>T, NM_001300856.1:c.404G>C, NM_001300857.2:c.296G>T, NM_001300857.2:c.296G>C, NM_001300857.1:c.296G>T, NM_001300857.1:c.296G>C, NP_005429.1:p.Cys201Phe, NP_005429.1:p.Cys201Ser, NP_001287773.1:p.Cys165Phe, NP_001287773.1:p.Cys165Ser, NP_001287785.1:p.Cys135Phe, NP_001287785.1:p.Cys135Ser, NP_001287786.1:p.Cys99Phe, NP_001287786.1:p.Cys99Ser

Select item 143381268220.

rs1433812682 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:65892996 (GRCh38)
11:65660467 (GRCh37)
Canonical SPDI:: NC_000011.10:65892995:T:C
Gene:: FOSL1 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.65892996T>C, NC_000011.9:g.65660467T>C, NG_047103.1:g.544A>G, NM_005438.5:c.706A>G, NM_005438.4:c.706A>G, NM_005438.3:c.706A>G, NM_001300855.2:c.*293A>G, NM_001300855.1:c.*293A>G, NM_001300844.2:c.598A>G, NM_001300844.1:c.598A>G, NR_125339.2:n.564A>G, NR_125339.1:n.545A>G, NM_001300856.2:c.508A>G, NM_001300856.1:c.508A>G, NM_001300857.2:c.400A>G, NM_001300857.1:c.400A>G, NP_005429.1:p.Thr236Ala, NP_001287773.1:p.Thr200Ala, NP_001287785.1:p.Thr170Ala, NP_001287786.1:p.Thr134Ala

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