Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005483.2 | 1790 | Intron | NP_005474.2 | ||
XM_011527605.2 | 1790 | Intron | XP_011525907.1 | ||
XM_011527606.2 | 1790 | Intron | XP_011525908.1 | ||
XM_011527607.2 | 1790 | Intron | XP_011525909.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171091.1 | 1790 | Missense Mutation | GCG,GTG | A368V | NP_001164562.1 |
NM_025241.2 | 1790 | Missense Mutation | GCG,GTG | A421V | NP_079517.1 |
XM_017027325.1 | 1790 | Missense Mutation | GCG,GTG | A455V | XP_016882814.1 |