Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142964.1 | 458 | Missense Mutation | CGG,TGG | R125W | NP_001136436.1 |
XM_011530373.2 | 458 | Missense Mutation | CGG,TGG | R125W | XP_011528675.1 |
XM_017028939.1 | 458 | UTR 5 | XP_016884428.1 |