Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318767.1 | 499 | Missense Mutation | GCT,GTT | A141V | NP_001305696.1 |
NM_001318768.1 | 499 | Missense Mutation | GCT,GTT | A141V | NP_001305697.1 |
NM_001318769.1 | 499 | Missense Mutation | GCT,GTT | A152V | NP_001305698.1 |
NM_001318770.1 | 499 | Missense Mutation | GCT,GTT | A194V | NP_001305699.1 |
NM_001318771.1 | 499 | Missense Mutation | GCT,GTT | A107V | NP_001305700.1 |
NM_032111.3 | 499 | Missense Mutation | GCT,GTT | A141V | NP_115487.2 |