Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001083885.2 | 3089 | Missense Mutation | GCG,GTG | A400V | NP_001077354.2 |
NM_001173425.1 | 3089 | Missense Mutation | GCG,GTG | A782V | NP_001166896.1 |
NM_015404.3 | 3089 | Missense Mutation | GCG,GTG | A783V | NP_056219.3 |
XM_011518484.1 | 3089 | Missense Mutation | GCG,GTG | A794V | XP_011516786.1 |
XM_011518485.1 | 3089 | Missense Mutation | GCG,GTG | A794V | XP_011516787.1 |
XM_011518486.1 | 3089 | Missense Mutation | GCG,GTG | A793V | XP_011516788.1 |
XM_011518487.1 | 3089 | Missense Mutation | GCG,GTG | A752V | XP_011516789.1 |
XM_011518488.1 | 3089 | Missense Mutation | GCG,GTG | A713V | XP_011516790.1 |
XM_011518489.2 | 3089 | Intron | XP_011516791.1 | ||
XM_011518491.2 | 3089 | Intron | XP_011516793.1 | ||
XM_011518492.1 | 3089 | Intron | XP_011516794.1 | ||
XM_011518494.2 | 3089 | Intron | XP_011516796.1 | ||
XM_011518495.1 | 3089 | Missense Mutation | GCG,GTG | A353V | XP_011516797.1 |