| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005650.3 | 6145 | Missense Mutation | ACC,GCC | T1942A | NP_005641.1 |
| NM_181492.2 | 6145 | Intron | NP_852469.1 | ||
| XM_005261722.3 | 6145 | Missense Mutation | ACC,GCC | T1942A | XP_005261779.1 |
| XM_006724313.3 | 6145 | Missense Mutation | ACC,GCC | T1942A | XP_006724376.1 |
| XM_011530353.2 | 6145 | Intron | XP_011528655.1 | ||
| XM_011530354.2 | 6145 | Intron | XP_011528656.1 |