Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099335.1 | 1666 | Missense Mutation | CGC,TGC | R277C | NP_001092805.1 |
NM_014759.3 | 1666 | Missense Mutation | CGC,TGC | R277C | NP_055574.3 |
XM_006716416.1 | 1666 | Missense Mutation | CGC,TGC | R277C | XP_006716479.1 |
XM_017014102.1 | 1666 | Missense Mutation | CGC,TGC | R144C | XP_016869591.1 |