Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281932.1 | 3447 | Intron | NP_001268861.1 | ||
NM_001281933.1 | 3447 | Missense Mutation | TAT,TGT | Y1148C | NP_001268862.1 |
NM_017760.6 | 3447 | Intron | NP_060230.5 | ||
XM_005249547.2 | 3447 | Intron | XP_005249604.1 | ||
XM_011516356.2 | 3447 | Missense Mutation | TAT,TGT | Y1148C | XP_011514658.1 |
XM_011516357.2 | 3447 | Missense Mutation | TAT,TGT | Y1148C | XP_011514659.1 |
XM_011516358.2 | 3447 | Intron | XP_011514660.1 | ||
XM_011516362.1 | 3447 | Intron | XP_011514664.1 | ||
XM_017012374.1 | 3447 | Missense Mutation | TAT,TGT | Y1101C | XP_016867863.1 |
XM_017012375.1 | 3447 | Missense Mutation | TAT,TGT | Y1090C | XP_016867864.1 |
XM_017012376.1 | 3447 | Intron | XP_016867865.1 | ||
XM_017012377.1 | 3447 | Missense Mutation | TAT,TGT | Y739C | XP_016867866.1 |
XM_017012378.1 | 3447 | Intron | XP_016867867.1 |