| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308277.1 | 509 | Missense Mutation | CCA,CTA | P67L | NP_001295206.1 |
| NM_018381.3 | 509 | Missense Mutation | CCA,CTA | P67L | NP_060851.2 |
| XM_011528121.1 | 509 | Missense Mutation | CCA,CTA | P28L | XP_011526423.1 |
| XM_011528122.1 | 509 | Intron | XP_011526424.1 | ||
| XM_017026934.1 | 509 | Missense Mutation | CCA,CTA | P16L | XP_016882423.1 |