Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001018009.3 | 1125 | Missense Mutation | CGG,TGG | R245W | NP_001018009.2 |
NM_004844.4 | 1125 | Missense Mutation | CGG,TGG | R402W | NP_004835.2 |
XM_011534251.2 | 1125 | Missense Mutation | CGG,TGG | R362W | XP_011532553.1 |
XM_011534253.1 | 1125 | Missense Mutation | CGG,TGG | R315W | XP_011532555.1 |
XM_017007521.1 | 1125 | Missense Mutation | CGG,TGG | R389W | XP_016863010.1 |
XM_017007522.1 | 1125 | Missense Mutation | CGG,TGG | R245W | XP_016863011.1 |
XM_017007523.1 | 1125 | Missense Mutation | CGG,TGG | R245W | XP_016863012.1 |
XM_017007524.1 | 1125 | Missense Mutation | CGG,TGG | R245W | XP_016863013.1 |
XM_017007525.1 | 1125 | Missense Mutation | CGG,TGG | R245W | XP_016863014.1 |