| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_182924.3 | 2811 | Missense Mutation | CCA,CTA | P896L | NP_891554.1 |
| XM_011515520.2 | 2811 | Silent Mutation | ACC,ACT | T894T | XP_011513822.1 |
| XM_011515522.2 | 2811 | Silent Mutation | ACC,ACT | T880T | XP_011513824.1 |
| XM_011515523.2 | 2811 | Silent Mutation | ACC,ACT | T811T | XP_011513825.1 |
| XM_011515524.2 | 2811 | Silent Mutation | ACC,ACT | T323T | XP_011513826.1 |
| XM_017012619.1 | 2811 | Intron | XP_016868108.1 |