Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018124.3 | 2317 | Missense Mutation | CGT,TGT | R756C | NP_060594.3 |
XM_005256021.4 | 2317 | Missense Mutation | CGT,TGT | R756C | XP_005256078.1 |
XM_005256022.4 | 2317 | Missense Mutation | CGT,TGT | R756C | XP_005256079.1 |
XM_006721228.3 | 2317 | Missense Mutation | CGT,TGT | R697C | XP_006721291.1 |
XM_011523191.2 | 2317 | Missense Mutation | CGT,TGT | R756C | XP_011521493.1 |
XM_017023391.1 | 2317 | Missense Mutation | CGT,TGT | R756C | XP_016878880.1 |
XM_017023392.1 | 2317 | Missense Mutation | CGT,TGT | R697C | XP_016878881.1 |