Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098514.2 | 1123 | Intron | NP_001091984.2 | ||
NM_152459.4 | 1123 | Missense Mutation | TCT,TGT | S322C | NP_689672.4 |
XM_005255143.3 | 1123 | Intron | XP_005255200.2 | ||
XM_011522392.2 | 1123 | Missense Mutation | TCT,TGT | S136C | XP_011520694.1 |
XM_017022972.1 | 1123 | Intron | XP_016878461.1 | ||
XM_017022973.1 | 1123 | UTR 3 | XP_016878462.1 | ||
XM_017022974.1 | 1123 | Intron | XP_016878463.1 |