| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130445.2 | 767 | Missense Mutation | CCA,TCA | P170S | NP_001123917.1 |
| NM_001287503.1 | 767 | Missense Mutation | CCA,TCA | P170S | NP_001274432.1 |
| NM_001287504.1 | 767 | Missense Mutation | CCA,TCA | P17S | NP_001274433.1 |
| NM_001287505.1 | 767 | Intron | NP_001274434.1 | ||
| NM_006751.6 | 767 | Missense Mutation | CCA,TCA | P170S | NP_006742.2 |
| XM_005246812.1 | 767 | Missense Mutation | CCA,TCA | P170S | XP_005246869.1 |
| XM_005246813.1 | 767 | Missense Mutation | CCA,TCA | P170S | XP_005246870.1 |
| XM_011511701.2 | 767 | Missense Mutation | CCA,TCA | P170S | XP_011510003.1 |
| XM_011511702.2 | 767 | Intron | XP_011510004.1 | ||
| XM_011511703.2 | 767 | Intron | XP_011510005.1 | ||
| XM_017004782.1 | 767 | Missense Mutation | CCA,TCA | P170S | XP_016860271.1 |