| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001560.2 | 560 | Missense Mutation | CCG,CTG | P80L | NP_001551.1 |
| XM_011531336.1 | 560 | Missense Mutation | CCG,CTG | P182L | XP_011529638.1 |
| XM_011531337.1 | 560 | Intron | XP_011529639.1 | ||
| XM_017029507.1 | 560 | Intron | XP_016884996.1 |