| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001324318.1 | 1869 | Missense Mutation | TCA,TTA | S609L | NP_001311247.1 |
| NM_001324319.1 | 1869 | Missense Mutation | TCA,TTA | S569L | NP_001311248.1 |
| NM_024745.4 | 1869 | Missense Mutation | TCA,TTA | S647L | NP_079021.3 |
| XM_011523335.2 | 1869 | Intron | XP_011521637.1 |