Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001035260.2 | 266 | Silent Mutation | TCC,TCT | S47S | NP_001030337.1 |
NM_001318944.1 | 266 | Missense Mutation | CCG,CTG | P5L | NP_001305873.1 |
NM_001318945.1 | 266 | Missense Mutation | CCG,CTG | P5L | NP_001305874.1 |
NM_001318946.1 | 266 | UTR 5 | NP_001305875.1 | ||
NM_004896.4 | 266 | Silent Mutation | TCC,TCT | S47S | NP_004887.2 |