| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317926.1 | 1031 | Missense Mutation | CGA,CTA | R183L | NP_001304855.1 |
| NM_013355.4 | 1031 | Missense Mutation | CGA,CTA | R183L | NP_037487.2 |
| XM_005251946.3 | 1031 | Missense Mutation | CGA,CTA | R180L | XP_005252003.1 |
| XM_006717080.2 | 1031 | Missense Mutation | CGA,CTA | R190L | XP_006717143.1 |
| XM_017014649.1 | 1031 | Missense Mutation | CGA,CTA | R190L | XP_016870138.1 |
| XM_017014650.1 | 1031 | Missense Mutation | CGA,CTA | R57L | XP_016870139.1 |