Homo sapiens serpin family C member 1 (SERPINC1), transcript variant 6 - Nucleotide

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[Phenotypic and genetic analysis of a Chinese pedigree affected with Hereditary antithrombin deficiency due to a novel variant of SERPINC1 gene]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Phenotypic and genetic analysis of a Chinese pedigree affected with Hereditary antithrombin deficiency due to a novel variant of SERPINC1 gene].
Chen Y, Yao Y, Li T, Shu K, Yang X, Li S, Wang X, Wang J, Zhang T, Jiang M. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Mar 10; 41(3):312-316.
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia. [Gene. 2024]
Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia.
Zhang K, Zhang H, Yu D, Pan J, Wang M, Xie H. Gene. 2024 Mar 1; 897:148085. Epub 2023 Dec 15.

RefSeq protein product
See the reference protein sequence for antithrombin-III isoform 6 precursor (NP_001373234.1).

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Protein sequence from Nucleotide coding region
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Homo sapiens serpin family C member 1 (SERPINC1), transcript variant 6, mRNA
Homo sapiens serpin family C member 1 (SERPINC1), transcript variant 6, mRNA
gi|1893772272|ref|NM_001386305.1|

Nucleotide

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Nucleotide