| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144856.1 | 1647 | Intron | NP_001138328.1 | ||
| NM_001144857.1 | 1647 | Intron | NP_001138329.1 | ||
| NM_018173.3 | 1647 | Intron | NP_060643.2 | ||
| XM_005253704.4 | 1647 | Intron | XP_005253761.1 | ||
| XM_006718985.3 | 1647 | Intron | XP_006719048.1 | ||
| XM_011520967.2 | 1647 | Intron | XP_011519269.1 | ||
| XM_017019555.1 | 1647 | Intron | XP_016875044.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001065.3 | 1647 | Silent Mutation | CCG,CCT | P448P | NP_001056.1 |