Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127218.2 | 1764 | Missense Mutation | CGT,TGT | R372C | NP_001120690.1 |
NM_001256879.1 | 1764 | Missense Mutation | CGT,TGT | R372C | NP_001243808.1 |
NM_006230.3 | 1764 | Missense Mutation | CGT,TGT | R407C | NP_006221.2 |
XM_011515431.1 | 1764 | Missense Mutation | CGT,TGT | R405C | XP_011513733.1 |