Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005459.3 | 615 | Missense Mutation | CGT,TGT | R183C | NP_005450.3 |
XM_005247910.3 | 615 | Missense Mutation | CCG,CTG | P196L | XP_005247967.1 |
XM_011513334.2 | 615 | Missense Mutation | CGT,TGT | R99C | XP_011511636.1 |