| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142797.1 | 807 | Missense Mutation | ACG,ATG | T260M | NP_001136269.1 |
| NM_001504.1 | 807 | Missense Mutation | ACG,ATG | T213M | NP_001495.1 |
| XM_005262256.3 | 807 | Missense Mutation | ACG,ATG | T223M | XP_005262313.1 |
| XM_005262257.3 | 807 | Intron | XP_005262314.1 | ||
| XM_017029435.1 | 807 | Missense Mutation | ACG,ATG | T260M | XP_016884924.1 |
| XM_017029436.1 | 807 | Intron | XP_016884925.1 |