| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001127197.1 | 2652 | Missense Mutation | CCA,CTA | P644L | NP_001120669.1 |
| NM_001421.3 | 2652 | Missense Mutation | CCA,CTA | P644L | NP_001412.1 |
| XM_005262389.3 | 2652 | Missense Mutation | CCA,CTA | P644L | XP_005262446.1 |
| XM_011531307.2 | 2652 | Missense Mutation | CCA,CTA | P576L | XP_011529609.1 |
| XM_011531308.2 | 2652 | Missense Mutation | CCA,CTA | P567L | XP_011529610.1 |