| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001933.1 | 675 | Missense Mutation | CCG,CTG | P4L | NP_001001933.1 |
| NM_001256114.1 | 675 | Intron | NP_001243043.1 | ||
| XM_017001316.1 | 675 | Intron | XP_016856805.1 | ||
| XM_017001317.1 | 675 | Intron | XP_016856806.1 |