Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001270780.1 | 582 | Missense Mutation | CGC,TGC | R181C | NP_001257709.1 |
NM_001270781.1 | 582 | Missense Mutation | CGC,TGC | R159C | NP_001257710.1 |
NM_033423.4 | 582 | Missense Mutation | CGC,TGC | R245C | NP_219491.1 |
XM_011536683.2 | 582 | Missense Mutation | CGC,TGC | R211C | XP_011534985.1 |