| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001103149.1 | 1726 | Missense Mutation | CCA,CGA | P377R | NP_001096619.1 |
| NM_018215.3 | 1726 | UTR 3 | NP_060685.2 | ||
| XM_011527067.2 | 1726 | Missense Mutation | CCA,CGA | P469R | XP_011525369.1 |