Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021822.3 | 721 | Missense Mutation | CGC,TGC | R122C | NP_068594.1 |
XM_006724290.1 | 721 | Missense Mutation | CGC,TGC | R55C | XP_006724353.1 |
XM_017028903.1 | 721 | Missense Mutation | CGC,TGC | R122C | XP_016884392.1 |
XM_017028904.1 | 721 | Missense Mutation | CGC,TGC | R55C | XP_016884393.1 |