Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114309.1 | 166 | Missense Mutation | CGT,TGT | R5C | NP_001107781.1 |
NM_004433.4 | 166 | Missense Mutation | CGT,TGT | R5C | NP_004424.3 |
XM_005244942.2 | 166 | Missense Mutation | CGT,TGT | R5C | XP_005244999.1 |