Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077239.1 | 248 | Missense Mutation | TCG,TTG | S47L | NP_001070707.1 |
NM_001278249.1 | 248 | Missense Mutation | TCG,TTG | S47L | NP_001265178.1 |
NM_207343.3 | 248 | Missense Mutation | TCG,TTG | S47L | NP_997226.2 |