Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166496.1 | 1648 | Missense Mutation | ATC,GTC | I429V | NP_001159968.1 |
NM_003051.3 | 1648 | Missense Mutation | ATC,GTC | I429V | NP_003042.3 |
XM_011542026.2 | 1648 | Intron | XP_011540328.1 | ||
XM_011542027.2 | 1648 | Intron | XP_011540329.1 |