Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001251969.1 | 411 | UTR 3 | NP_001238898.1 | ||
NM_022902.4 | 411 | Missense Mutation | CGG,TGG | R92W | NP_075053.2 |
NM_024055.4 | 411 | UTR 3 | NP_076960.1 | ||
XM_005248569.3 | 411 | Missense Mutation | CGG,TGG | R51W | XP_005248626.1 |
XM_006714672.3 | 411 | Missense Mutation | CGG,TGG | R92W | XP_006714735.1 |
XM_017009749.1 | 411 | Missense Mutation | CGG,TGG | R51W | XP_016865238.1 |