Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206855.1 | 2358 | Missense Mutation | CGG,TGG | R602W | NP_001193784.1 |
NM_003227.3 | 2358 | Missense Mutation | CGG,TGG | R773W | NP_003218.2 |
XM_005250553.4 | 2358 | Missense Mutation | CGG,TGG | R773W | XP_005250610.1 |
XM_017012573.1 | 2358 | Missense Mutation | CGG,TGG | R773W | XP_016868062.1 |