Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282450.1 | 1176 | Intron | NP_001269379.1 | ||
NM_001282451.1 | 1176 | Missense Mutation | CGG,TGG | R319W | NP_001269380.1 |
NM_004451.4 | 1176 | Missense Mutation | CGG,TGG | R320W | NP_004442.3 |
XM_017017313.1 | 1176 | Missense Mutation | CGG,TGG | R330W | XP_016872802.1 |