asparaginyl-tRNA synthetase isoform 2 [Rattus norvegicus]

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Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. [PLoS Genet. 2015]
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
Simon M, Richard EM, Wang X, Shahzad M, Huang VH, Qaiser TA, Potluri P, Mahl SE, Davila A, Nazli S, et al. PLoS Genet. 2015 Mar; 11(3):e1005097. Epub 2015 Mar 25.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.
A mitochondrial protein compendium elucidates complex I disease biology. [Cell. 2008]
A mitochondrial protein compendium elucidates complex I disease biology.
Pagliarini DJ, Calvo SE, Chang B, Sheth SA, Vafai SB, Ong SE, Walford GA, Sugiana C, Boneh A, Chen WK, et al. Cell. 2008 Jul 11; 134(1):112-23.

RefSeq mRNA
See reference mRNA sequence for the Nars2 gene (NM_001034921.2).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the Nars2 gene.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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