Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142293.1 | 1689 | Missense Mutation | CAG,CGG | Q446R | NP_001135765.1 |
NM_014570.4 | 1689 | Missense Mutation | CAG,CGG | Q490R | NP_055385.3 |
XM_005261525.3 | 1689 | Missense Mutation | CAG,CGG | Q446R | XP_005261582.1 |