| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286691.1 | 1727 | Missense Mutation | CCA,CTA | P555L | NP_001273620.1 |
| NM_004529.3 | 1727 | Missense Mutation | CCA,CTA | P558L | NP_004520.2 |
| XM_017014726.1 | 1727 | Missense Mutation | CCA,CTA | P510L | XP_016870215.1 |
| XM_017014727.1 | 1727 | Missense Mutation | CCA,CTA | P507L | XP_016870216.1 |