Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020812.3 | 5708 | Missense Mutation | CGT,TGT | R1872C | NP_065863.2 |
XM_005260000.2 | 5708 | Missense Mutation | CGT,TGT | R1938C | XP_005260057.1 |
XM_005260001.2 | 5708 | Missense Mutation | CGT,TGT | R1907C | XP_005260058.1 |
XM_006722804.3 | 5708 | Missense Mutation | CGT,TGT | R984C | XP_006722867.1 |
XM_011528150.1 | 5708 | Missense Mutation | CGT,TGT | R1918C | XP_011526452.1 |
XM_011528151.1 | 5708 | Missense Mutation | CGT,TGT | R1914C | XP_011526453.1 |
XM_011528152.1 | 5708 | Missense Mutation | CGT,TGT | R1883C | XP_011526454.1 |