Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013432.4 | 3578 | Missense Mutation | GCT,GTT | A1188V | NP_038460.4 |
XM_011517048.2 | 3578 | Missense Mutation | GCT,GTT | A864V | XP_011515350.1 |
XM_011517049.2 | 3578 | Missense Mutation | GCT,GTT | A852V | XP_011515351.1 |
XM_011517050.2 | 3578 | Intron | XP_011515352.1 |