| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008225.2 | 2465 | Intron | NP_001008226.1 | ||
| NM_001190847.1 | 2465 | Missense Mutation | CGC,TGC | R641C | NP_001177776.1 |
| NM_001190848.1 | 2465 | Intron | NP_001177777.1 | ||
| NM_001190849.1 | 2465 | Missense Mutation | CGC,TGC | R709C | NP_001177778.1 |
| NM_001190850.1 | 2465 | Missense Mutation | CGC,TGC | R712C | NP_001177779.1 |
| NM_013316.3 | 2465 | Missense Mutation | CGC,TGC | R638C | NP_037448.2 |
| XM_017012235.1 | 2465 | Missense Mutation | CGC,TGC | R712C | XP_016867724.1 |