Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281450.1 | 1067 | Missense Mutation | ACG,ATG | T313M | NP_001268379.1 |
NM_001281451.1 | 1067 | Missense Mutation | ACG,ATG | T314M | NP_001268380.1 |
NM_178125.3 | 1067 | Missense Mutation | ACG,ATG | T314M | NP_835226.2 |
XM_011515787.1 | 1067 | UTR 3 | XP_011514089.1 | ||
XM_011515788.2 | 1067 | Missense Mutation | ACG,ATG | T105M | XP_011514090.1 |
XM_011515789.2 | 1067 | Missense Mutation | ACG,ATG | T313M | XP_011514091.2 |