| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001013031.2 | 3790 | Intron | NP_001013049.1 | ||
| NM_001206569.1 | 3790 | Intron | NP_001193498.1 | ||
| NM_001206570.1 | 3790 | Intron | NP_001193499.1 | ||
| NM_001206571.1 | 3790 | Intron | NP_001193500.1 | ||
| NM_001206572.1 | 3790 | UTR 3 | NP_001193501.1 | ||
| NM_052918.4 | 3790 | Missense Mutation | AGA,AGC | R1149S | NP_443150.3 |
| XM_011539199.2 | 3790 | Intron | XP_011537501.1 | ||
| XM_011539201.2 | 3790 | Intron | XP_011537503.1 | ||
| XM_017015614.1 | 3790 | Intron | XP_016871103.1 | ||
| XM_017015615.1 | 3790 | Intron | XP_016871104.1 | ||
| XM_017015616.1 | 3790 | Intron | XP_016871105.1 | ||
| XM_017015617.1 | 3790 | Intron | XP_016871106.1 | ||
| XM_017015618.1 | 3790 | Intron | XP_016871107.1 |