Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318391.1 | 469 | Missense Mutation | CGG,TGG | R60W | NP_001305320.1 |
NM_032830.2 | 469 | Missense Mutation | CGG,TGG | R143W | NP_116219.2 |
XM_005256205.3 | 469 | Intron | XP_005256262.2 |