Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256269.1 | 626 | Missense Mutation | CCG,TCG | P80S | NP_001243198.1 |
NM_001256270.1 | 626 | Missense Mutation | CCG,TCG | P80S | NP_001243199.1 |
NM_007317.2 | 626 | Missense Mutation | CCG,TCG | P148S | NP_015556.1 |