| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145649.1 | 1458 | Intron | NP_001139121.1 | ||
| NM_001145650.1 | 1458 | Intron | NP_001139122.1 | ||
| NM_001321351.1 | 1458 | Intron | NP_001308280.1 | ||
| NM_020951.4 | 1458 | Intron | NP_066002.3 | ||
| XM_006723302.3 | 1458 | Intron | XP_006723365.1 | ||
| XM_006723304.2 | 1458 | Intron | XP_006723367.1 | ||
| XM_011527164.2 | 1458 | Intron | XP_011525466.1 | ||
| XM_011527165.2 | 1458 | Intron | XP_011525467.1 | ||
| XM_011527166.2 | 1458 | Intron | XP_011525468.1 | ||
| XM_011527167.2 | 1458 | Intron | XP_011525469.1 | ||
| XM_011527169.2 | 1458 | Missense Mutation | GAT,GGT | D419G | XP_011525471.1 |
| XM_011527170.1 | 1458 | Intron | XP_011525472.1 | ||
| XM_017027039.1 | 1458 | Intron | XP_016882528.1 | ||
| XM_017027040.1 | 1458 | Intron | XP_016882529.1 | ||
| XM_017027041.1 | 1458 | Intron | XP_016882530.1 | ||
| XM_017027042.1 | 1458 | Intron | XP_016882531.1 | ||
| XM_017027043.1 | 1458 | Intron | XP_016882532.1 | ||
| XM_017027044.1 | 1458 | Intron | XP_016882533.1 | ||
| XM_017027045.1 | 1458 | Intron | XP_016882534.1 |