Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099436.3 | 928 | Missense Mutation | CGT,TGT | R257C | NP_001092906.3 |
NM_001284364.2 | 928 | Missense Mutation | CGT,TGT | R257C | NP_001271293.2 |
NM_001284365.2 | 928 | Missense Mutation | CGT,TGT | R140C | NP_001271294.1 |
XM_005254289.2 | 928 | Missense Mutation | CGT,TGT | R268C | XP_005254346.1 |
XM_017022068.1 | 928 | Missense Mutation | CGT,TGT | R268C | XP_016877557.1 |
XM_017022069.1 | 928 | Missense Mutation | CGT,TGT | R167C | XP_016877558.1 |
XM_017022070.1 | 928 | Missense Mutation | CGT,TGT | R167C | XP_016877559.1 |
XM_017022071.1 | 928 | Missense Mutation | CGT,TGT | R167C | XP_016877560.1 |
XM_017022072.1 | 928 | Missense Mutation | CGT,TGT | R167C | XP_016877561.1 |