Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001306079.1 | 466 | Missense Mutation | CGC,TGC | R102C | NP_001293008.1 |
NM_004341.4 | 466 | Missense Mutation | CGC,TGC | R102C | NP_004332.2 |
XM_005264555.3 | 466 | Missense Mutation | CGC,TGC | R102C | XP_005264612.1 |
XM_006712101.2 | 466 | Missense Mutation | CGC,TGC | R102C | XP_006712164.1 |