Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042465.2 | 1655 | Missense Mutation | CCA,TCA | P502S | NP_001035930.1 |
NM_001042466.2 | 1655 | Missense Mutation | CCA,TCA | P501S | NP_001035931.1 |
NM_002778.3 | 1655 | Missense Mutation | CCA,TCA | P499S | NP_002769.1 |