Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001038.5 | 2294 | Missense Mutation | TGC,TTC | C618F | NP_001029.1 |
NM_001159575.1 | 2294 | Missense Mutation | TGC,TTC | C641F | NP_001153047.1 |
NM_001159576.1 | 2294 | Missense Mutation | TGC,TTC | C677F | NP_001153048.1 |