Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_175078.2 | 1152 | Missense Mutation | GCG,GGG | A454G | NP_778253.2 |
XM_011538288.2 | 1152 | Missense Mutation | GCG,GGG | A221G | XP_011536590.1 |
XM_011538289.2 | 1152 | Intron | XP_011536591.1 |