| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001874.2 | 667 | Intron | NP_001001874.1 | ||
| NM_001001875.3 | 667 | Intron | NP_001001875.1 | ||
| NM_033516.5 | 667 | Silent Mutation | CCC,CCG | P140P | NP_277051.3 |
| XM_017015280.1 | 667 | Intron | XP_016870769.1 |