| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012643.3 | 635 | Missense Mutation | GCC,GGC | A183G | NP_001012661.1 |
| XM_017026742.1 | 635 | Missense Mutation | GCC,GGC | A326G | XP_016882231.1 |
| XM_017026743.1 | 635 | Missense Mutation | CCC,GCC | P363A | XP_016882232.1 |