| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003850.2 | 1538 | Missense Mutation | ACG,GCG | T421A | NP_003841.1 |
| XM_017020806.1 | 1538 | Missense Mutation | ACG,GCG | T363A | XP_016876295.1 |
| XM_017020807.1 | 1538 | Missense Mutation | ACG,GCG | T342A | XP_016876296.1 |
| XM_017020808.1 | 1538 | Intron | XP_016876297.1 | ||
| XM_017020809.1 | 1538 | Missense Mutation | ACG,GCG | T287A | XP_016876298.1 |