Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_031231.3 | 677 | Missense Mutation | CGG,TGG | R191W | NP_112508.3 |
NM_031232.3 | 677 | Missense Mutation | CGG,TGG | R191W | NP_112509.3 |
XM_005260510.1 | 677 | Missense Mutation | CGG,TGG | R191W | XP_005260567.1 |
XM_011528991.1 | 677 | Missense Mutation | CGG,TGG | R30W | XP_011527293.1 |
XM_011528992.2 | 677 | UTR 3 | XP_011527294.1 | ||
XM_017028015.1 | 677 | Missense Mutation | CGG,TGG | R30W | XP_016883504.1 |
XM_017028016.1 | 677 | Missense Mutation | CGG,TGG | R30W | XP_016883505.1 |