Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001694.2 | 2166 | Missense Mutation | CGC,TGC | R257C | NP_001001694.2 |
XM_011530689.2 | 2166 | Missense Mutation | CGC,TGC | R329C | XP_011528991.1 |
XM_017028798.1 | 2166 | Missense Mutation | CGC,TGC | R329C | XP_016884287.1 |