Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193314.1 | 1362 | Missense Mutation | CGG,TGG | R455W | NP_001180243.1 |
NM_001193315.1 | 1362 | Missense Mutation | CGG,TGG | R455W | NP_001180244.1 |
NM_001193316.1 | 1362 | Missense Mutation | CGG,TGG | R406W | NP_001180245.1 |
NM_001193317.1 | 1362 | Missense Mutation | CGG,TGG | R455W | NP_001180246.1 |
NM_022067.3 | 1362 | Missense Mutation | CGG,TGG | R455W | NP_071350.2 |
XM_011537066.1 | 1362 | Missense Mutation | CGG,TGG | R424W | XP_011535368.1 |
XM_017021579.1 | 1362 | Missense Mutation | CGG,TGG | R424W | XP_016877068.1 |
XM_017021580.1 | 1362 | Intron | XP_016877069.1 | ||
XM_017021581.1 | 1362 | Intron | XP_016877070.1 |