Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_139025.4 | 580 | Missense Mutation | ATG,GTG | M46V | NP_620594.1 |
NM_139026.4 | 580 | Missense Mutation | ATG,GTG | M46V | NP_620595.1 |
NM_139027.4 | 580 | Missense Mutation | ATG,GTG | M46V | NP_620596.2 |
XM_011518176.2 | 580 | Intron | XP_011516478.1 | ||
XM_011518178.1 | 580 | Intron | XP_011516480.1 | ||
XM_011518179.1 | 580 | Intron | XP_011516481.1 | ||
XM_017014232.1 | 580 | Missense Mutation | ATG,GTG | M42V | XP_016869721.1 |
XM_017014233.1 | 580 | UTR 5 | XP_016869722.1 | ||
XM_017014234.1 | 580 | Intron | XP_016869723.1 | ||
XM_017014235.1 | 580 | Missense Mutation | ATG,GTG | M46V | XP_016869724.1 |