| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242673.1 | 315 | UTR 5 | NP_001229602.1 | ||
| NM_001242674.1 | 315 | Intron | NP_001229603.1 | ||
| NM_001242675.1 | 315 | Intron | NP_001229604.1 | ||
| NM_001242676.1 | 315 | Intron | NP_001229605.1 | ||
| NM_006621.5 | 315 | Missense Mutation | CCG,CTG | P9L | NP_006612.2 |
| XM_011540535.1 | 315 | Missense Mutation | CCG,CTG | P9L | XP_011538837.1 |