Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001288732.1 | 3441 | Missense Mutation | TAT,TGT | Y1099C | NP_001275661.1 |
NM_001288733.1 | 3441 | Missense Mutation | TAT,TGT | Y1099C | NP_001275662.1 |
NM_018469.4 | 3441 | Missense Mutation | TAT,TGT | Y1106C | NP_060939.3 |
XM_011524998.1 | 3441 | Missense Mutation | TAT,TGT | Y1106C | XP_011523300.1 |
XM_011524999.1 | 3441 | Missense Mutation | TAT,TGT | Y1106C | XP_011523301.1 |
XM_011525000.1 | 3441 | Missense Mutation | TAT,TGT | Y1104C | XP_011523302.1 |
XM_017024846.1 | 3441 | Missense Mutation | TAT,TGT | Y1097C | XP_016880335.1 |
XM_017024847.1 | 3441 | Intron | XP_016880336.1 |