Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301030.1 | 3914 | Missense Mutation | GCG,GTG | A821V | NP_001287959.1 |
NM_002088.4 | 3914 | Missense Mutation | GCG,GTG | A821V | NP_002079.3 |
XM_005258821.3 | 3914 | Missense Mutation | GCG,GTG | A821V | XP_005258878.1 |
XM_011526862.2 | 3914 | Missense Mutation | GCG,GTG | A822V | XP_011525164.1 |
XM_011526863.2 | 3914 | Missense Mutation | GCG,GTG | A821V | XP_011525165.1 |
XM_011526865.1 | 3914 | Missense Mutation | GCG,GTG | A822V | XP_011525167.1 |
XM_011526867.1 | 3914 | Missense Mutation | GCG,GTG | A753V | XP_011525169.1 |
XM_011526868.1 | 3914 | Missense Mutation | GCG,GTG | A741V | XP_011525170.1 |
XM_011526869.2 | 3914 | Intron | XP_011525171.1 | ||
XM_011526870.2 | 3914 | Intron | XP_011525172.1 | ||
XM_011526871.2 | 3914 | Intron | XP_011525173.1 | ||
XM_017026713.1 | 3914 | Missense Mutation | GCG,GTG | A754V | XP_016882202.1 |