| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001128631.2 | 952 | Missense Mutation | TCC,TTC | S199F | NP_001122103.1 |
| NM_001288654.2 | 952 | Missense Mutation | TCC,TTC | S199F | NP_001275583.1 |
| NM_001288655.1 | 952 | Missense Mutation | TCC,TTC | S199F | NP_001275584.1 |
| NM_001321326.1 | 952 | Missense Mutation | TCC,TTC | S199F | NP_001308255.1 |
| NM_024819.6 | 952 | Missense Mutation | TCC,TTC | S199F | NP_079095.3 |
| XM_005257688.2 | 952 | Intron | XP_005257745.1 | ||
| XM_011525262.2 | 952 | Missense Mutation | TCC,TTC | S199F | XP_011523564.1 |
| XM_017025102.1 | 952 | Intron | XP_016880591.1 | ||
| XM_017025103.1 | 952 | Intron | XP_016880592.1 | ||
| XM_017025104.1 | 952 | Intron | XP_016880593.1 | ||
| XM_017025105.1 | 952 | Missense Mutation | TCC,TTC | S98F | XP_016880594.1 |
| XM_017025106.1 | 952 | Missense Mutation | TCC,TTC | S98F | XP_016880595.1 |