Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145652.3 | 291 | Missense Mutation | CGC,TGC | R68C | NP_663627.1 |
XM_011528601.1 | 291 | Missense Mutation | CGC,TGC | R68C | XP_011526903.1 |
XM_011528602.1 | 291 | Missense Mutation | CGC,TGC | R68C | XP_011526904.1 |