Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000939.3 | 798 | Missense Mutation | CCG,GCG | P132A | NP_000930.1 |
NM_001035256.2 | 798 | Missense Mutation | CCG,GCG | P132A | NP_001030333.1 |
NM_001319204.1 | 798 | Missense Mutation | CCG,GCG | P132A | NP_001306133.1 |
NM_001319205.1 | 798 | Missense Mutation | CCG,GCG | P132A | NP_001306134.1 |