| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267713.1 | 464 | Intron | NP_001254642.1 | ||
| NM_002183.3 | 464 | Missense Mutation | CCA,CTA | P26L | NP_002174.1 |
| XM_005274431.4 | 464 | Missense Mutation | CCA,CTA | P26L | XP_005274488.1 |
| XM_005274432.1 | 464 | Missense Mutation | CCA,CTA | P26L | XP_005274489.1 |
| XM_017029491.1 | 464 | Missense Mutation | CCA,CTA | P26L | XP_016884980.1 |