| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001013627.2 | 1829 | Intron | NP_001013649.2 | ||
| XM_011530932.1 | 1829 | Intron | XP_011529234.1 | ||
| XM_011530933.1 | 1829 | Intron | XP_011529235.1 | ||
| XM_011530934.2 | 1829 | Intron | XP_011529236.1 | ||
| XM_017029473.1 | 1829 | Intron | XP_016884962.1 | ||
| XM_017029474.1 | 1829 | Intron | XP_016884963.1 | ||
| XM_017029475.1 | 1829 | Intron | XP_016884964.1 | ||
| XM_017029476.1 | 1829 | Intron | XP_016884965.1 | ||
| XM_017029477.1 | 1829 | Intron | XP_016884966.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024455.3 | 1829 | Missense Mutation | CCC,GCC | P490A | NP_001019626.1 |