Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204897.1 | 692 | Missense Mutation | CCG,CTG | P177L | NP_001191826.1 |
NM_001204898.1 | 692 | Silent Mutation | TCC,TCT | S152S | NP_001191827.1 |
NM_138461.3 | 692 | Silent Mutation | TCC,TCT | S178S | NP_612470.2 |