| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002974.3 | 632 | Missense Mutation | CCA,CTA | P162L | NP_002965.1 |
| NM_175041.1 | 632 | Missense Mutation | CCA,CTA | P162L | NP_778206.1 |
| XM_011526138.1 | 632 | Missense Mutation | CCA,CTA | P162L | XP_011524440.1 |