Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002217.3 | 133 | Missense Mutation | CGG,TGG | R33W | NP_002208.3 |
XM_005265105.4 | 133 | Missense Mutation | CGG,TGG | R33W | XP_005265162.1 |
XM_017006356.1 | 133 | Intron | XP_016861845.1 |