| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171971.2 | 170 | Missense Mutation | CGC,CTC | R15L | NP_001165442.1 |
| NM_033100.3 | 170 | Missense Mutation | CGC,CTC | R15L | NP_149091.1 |
| XM_011540337.1 | 170 | Intron | XP_011538639.1 | ||
| XM_011540338.1 | 170 | Intron | XP_011538640.1 | ||
| XM_011540339.1 | 170 | UTR 5 | XP_011538641.1 | ||
| XM_011540340.2 | 170 | Intron | XP_011538642.1 |