Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206833.1 | 556 | Intron | NP_001193762.1 | ||
NM_006388.3 | 556 | Missense Mutation | GCC,GTC | A97V | NP_006379.2 |
NM_182709.2 | 556 | Intron | NP_874368.1 | ||
NM_182710.2 | 556 | Missense Mutation | GCC,GTC | A130V | NP_874369.1 |
XM_006718421.2 | 556 | Missense Mutation | GCC,GTC | A106V | XP_006718484.1 |