Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114133.2 | 2147 | Missense Mutation | GCT,GTT | A944V | NP_001107605.1 |
NM_024875.4 | 2147 | Missense Mutation | GCT,GTT | A720V | NP_079151.2 |
XM_005270158.2 | 2147 | Missense Mutation | GCT,GTT | A648V | XP_005270215.1 |
XM_005270159.3 | 2147 | Missense Mutation | GCT,GTT | A648V | XP_005270216.1 |