Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278562.1 | 1598 | Missense Mutation | GCT,GTT | A316V | NP_001265491.1 |
NM_207338.3 | 1598 | Missense Mutation | GCT,GTT | A489V | NP_997221.2 |
XM_017021999.1 | 1598 | Missense Mutation | GCT,GTT | A506V | XP_016877488.1 |