| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271842.1 | 392 | Missense Mutation | CCA,CTA | P89L | NP_001258771.1 |
| NM_001319190.1 | 392 | Intron | NP_001306119.1 | ||
| NM_207103.3 | 392 | Missense Mutation | CCA,CTA | P96L | NP_996986.1 |
| XM_017024615.1 | 392 | Intron | XP_016880104.1 |