Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001115.2 | 3770 | Missense Mutation | CGG,TGG | R1129W | NP_001106.1 |
XM_005250769.3 | 3770 | Missense Mutation | CGG,TGG | R1099W | XP_005250826.1 |
XM_006716501.3 | 3770 | Missense Mutation | CGG,TGG | R1063W | XP_006716564.1 |
XM_017013006.1 | 3770 | Missense Mutation | CGG,TGG | R1033W | XP_016868495.1 |
XM_017013007.1 | 3770 | Intron | XP_016868496.1 |