Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001083613.1 | 579 | Missense Mutation | GCT,GTT | A147V | NP_001077082.1 |
NM_194280.3 | 579 | Missense Mutation | GCT,GTT | A147V | NP_919256.1 |
XM_005255123.1 | 579 | Missense Mutation | GCT,GTT | A147V | XP_005255180.1 |