Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001242597.1 | 448 | Missense Mutation | GCC,GTC | A128V | NP_001229526.1 |
NM_001242598.1 | 448 | Missense Mutation | GCC,GTC | A103V | NP_001229527.1 |
NM_032635.3 | 448 | Missense Mutation | GCC,GTC | A177V | NP_116024.1 |