| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004426.2 | 529 | Intron | NP_004417.2 | ||
| XM_005253334.2 | 529 | Intron | XP_005253391.1 | ||
| XM_011520599.2 | 529 | Intron | XP_011518901.1 | ||
| XM_011520600.2 | 529 | Intron | XP_011518902.1 | ||
| XM_011520603.2 | 529 | Intron | XP_011518905.1 | ||
| XM_017018955.1 | 529 | Missense Mutation | AAT,AGT | N10S | XP_016874444.1 |
| XM_017018956.1 | 529 | Intron | XP_016874445.1 | ||
| XM_017018957.1 | 529 | Intron | XP_016874446.1 | ||
| XM_017018958.1 | 529 | Intron | XP_016874447.1 |