| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001006639.1 | 362 | Missense Mutation | CGC,CTC | R67L | NP_001006640.1 |
| NM_001006640.1 | 362 | Missense Mutation | CGC,CTC | R67L | NP_001006641.1 |
| NM_004780.2 | 362 | Missense Mutation | CGC,CTC | R67L | NP_004771.2 |