Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001017415.1 | 332 | Missense Mutation | CCT,TCT | P2S | NP_001017415.1 |
NM_001017416.1 | 332 | Missense Mutation | CCT,TCT | P2S | NP_001017416.1 |
NM_003368.4 | 332 | Missense Mutation | CCT,TCT | P2S | NP_003359.3 |