| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001023570.3 | 1280 | Intron | NP_001018864.2 | ||
| NM_001023571.3 | 1280 | Intron | NP_001018865.2 | ||
| NM_001319107.1 | 1280 | Intron | NP_001306036.1 | ||
| XM_005247911.3 | 1280 | Intron | XP_005247968.1 | ||
| XM_005247912.2 | 1280 | Intron | XP_005247969.1 | ||
| XM_011513335.2 | 1280 | Intron | XP_011511637.1 | ||
| XM_017007537.1 | 1280 | Intron | XP_016863026.1 | ||
| XM_017007538.1 | 1280 | Nonsense Mutation | CGA,TGA | R277* | XP_016863027.1 |
| XM_017007539.1 | 1280 | Intron | XP_016863028.1 |