| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171020.1 | 879 | Missense Mutation | CCA,CTA | P79L | NP_001164491.1 |
| NM_152423.4 | 879 | Missense Mutation | CCA,CTA | P79L | NP_689636.3 |
| XM_005262077.2 | 879 | Missense Mutation | CCA,CTA | P79L | XP_005262134.1 |
| XM_011530856.1 | 879 | Missense Mutation | CCA,CTA | P79L | XP_011529158.1 |
| XM_011530857.1 | 879 | Missense Mutation | CCA,CTA | P79L | XP_011529159.1 |
| XM_017029269.1 | 879 | Missense Mutation | CCA,CTA | P79L | XP_016884758.1 |