| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001160210.1 | 1695 | Missense Mutation | CCT,TCT | P541S | NP_001153682.1 |
| NM_014251.2 | 1695 | Missense Mutation | CCT,TCT | P540S | NP_055066.1 |
| XM_006715831.3 | 1695 | Missense Mutation | CCT,TCT | P551S | XP_006715894.1 |
| XM_011515727.2 | 1695 | Intron | XP_011514029.1 | ||
| XM_017011663.1 | 1695 | Missense Mutation | CCT,TCT | P537S | XP_016867152.1 |
| XM_017011664.1 | 1695 | Missense Mutation | CCT,TCT | P256S | XP_016867153.1 |
| XM_017011665.1 | 1695 | Missense Mutation | CCT,TCT | P256S | XP_016867154.1 |