| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001131034.3 | 627 | Intron | NP_001124506.1 | ||
| NM_001193318.2 | 627 | Intron | NP_001180247.1 | ||
| NM_194439.4 | 627 | Intron | NP_919420.1 | ||
| XM_005272274.2 | 627 | Missense Mutation | CCC,TCC | P263S | XP_005272331.1 |
| XM_011513439.1 | 627 | Intron | XP_011511741.1 | ||
| XM_011513443.1 | 627 | Intron | XP_011511745.1 | ||
| XM_011513444.1 | 627 | Intron | XP_011511746.1 | ||
| XM_011513445.2 | 627 | Intron | XP_011511747.1 | ||
| XM_011513446.1 | 627 | Missense Mutation | CCC,TCC | P175S | XP_011511748.1 |
| XM_017008039.1 | 627 | Intron | XP_016863528.1 | ||
| XM_017008040.1 | 627 | Intron | XP_016863529.1 | ||
| XM_017008041.1 | 627 | Intron | XP_016863530.1 | ||
| XM_017008042.1 | 627 | Intron | XP_016863531.1 |