Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001190992.1 | 1813 | Missense Mutation | GCT,GTT | A423V | NP_001177921.1 |
NM_004733.3 | 1813 | Missense Mutation | GCT,GTT | A423V | NP_004724.1 |
XM_011513311.2 | 1813 | Missense Mutation | GCT,GTT | A322V | XP_011511613.1 |
XM_017007462.1 | 1813 | Missense Mutation | GCT,GTT | A321V | XP_016862951.1 |
XM_017007463.1 | 1813 | Missense Mutation | GCT,GTT | A253V | XP_016862952.1 |
XM_017007464.1 | 1813 | Missense Mutation | GCT,GTT | A152V | XP_016862953.1 |