Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138961.2 | 751 | Missense Mutation | GCT,GTT | A386V | NP_620411.2 |
XM_005271720.4 | 751 | Missense Mutation | GCT,GTT | A207V | XP_005271777.1 |
XM_011543060.2 | 751 | Missense Mutation | GCT,GTT | A283V | XP_011541362.1 |