Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152280.4 | 579 | Missense Mutation | CGT,TGT | R91C | NP_689493.3 |
XM_005245014.2 | 579 | Missense Mutation | CGT,TGT | R91C | XP_005245071.1 |
XM_017000759.1 | 579 | Missense Mutation | CGT,TGT | R91C | XP_016856248.1 |