Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166695.2 | 292 | Missense Mutation | AGT,CGT | S23R | NP_001160167.1 |
NM_001166696.2 | 292 | Missense Mutation | AGT,CGT | S23R | NP_001160168.1 |
NM_001289939.1 | 292 | Missense Mutation | AGT,CGT | S23R | NP_001276868.1 |
NM_001289940.1 | 292 | Missense Mutation | AGT,CGT | S23R | NP_001276869.1 |
NM_004172.4 | 292 | Missense Mutation | AGT,CGT | S23R | NP_004163.3 |
XM_005248342.2 | 292 | Missense Mutation | AGT,CGT | S23R | XP_005248399.1 |
XM_011514084.2 | 292 | UTR 5 | XP_011512386.1 |