Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013743.2 | 940 | Missense Mutation | CGT,TGT | R201C | NP_001013765.2 |
XM_006718832.3 | 940 | Missense Mutation | CGT,TGT | R151C | XP_006718895.1 |
XM_011542802.2 | 940 | Missense Mutation | CGT,TGT | R156C | XP_011541104.1 |
XM_017017653.1 | 940 | Intron | XP_016873142.1 |