Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005981.3 | 1176 | Missense Mutation | CGG,TGG | R33W | NP_005972.1 |
XM_005269074.3 | 1176 | Missense Mutation | CGG,TGG | R123W | XP_005269131.2 |
XM_017019793.1 | 1176 | Intron | XP_016875282.1 |