HapMap
HapMap
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130860.3 | 295 | Intron | NP_001124332.1 | ||
| NM_001282141.1 | 295 | Intron | NP_001269070.1 | ||
| NM_014799.3 | 295 | Intron | NP_055614.1 | ||
| NM_138737.4 | 295 | Missense Mutation | GCG,GTG | A39V | NP_620074.3 |
| XM_006724722.1 | 295 | Intron | XP_006724785.1 | ||
| XM_011531073.2 | 295 | Missense Mutation | GCG,GTG | A39V | XP_011529375.1 |
| XM_011531074.2 | 295 | Missense Mutation | GCG,GTG | A39V | XP_011529376.1 |
| XM_011531075.2 | 295 | Missense Mutation | GCG,GTG | A39V | XP_011529377.1 |
| XM_017029998.1 | 295 | Missense Mutation | GCG,GTG | A39V | XP_016885487.1 |
| XM_017029999.1 | 295 | Intron | XP_016885488.1 | ||
| XM_017030000.1 | 295 | Intron | XP_016885489.1 | ||
| XM_017030001.1 | 295 | Intron | XP_016885490.1 | ||
| XM_017030002.1 | 295 | Intron | XP_016885491.1 | ||
| XM_017030003.1 | 295 | Intron | XP_016885492.1 |