Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204897.1 | 678 | Silent Mutation | ACA,ACG | T172T | NP_001191826.1 |
NM_001204898.1 | 678 | Missense Mutation | ATG,GTG | M148V | NP_001191827.1 |
NM_138461.3 | 678 | Missense Mutation | ATG,GTG | M174V | NP_612470.2 |