Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079870.1 | 1763 | Missense Mutation | GCC,GTC | A592V | NP_001073339.1 |
NM_001079871.1 | 1763 | Missense Mutation | GCC,GTC | A584V | NP_001073340.1 |
NM_177977.2 | 1763 | Missense Mutation | GCC,GTC | A609V | NP_817084.2 |