| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001260486.1 | 1768 | Intron | NP_001247415.1 | ||
| NM_001260487.1 | 1768 | Intron | NP_001247416.1 | ||
| NM_001260488.1 | 1768 | Intron | NP_001247417.1 | ||
| NM_003445.3 | 1768 | Intron | NP_003436.3 | ||
| NM_198089.2 | 1768 | Intron | NP_932355.2 | ||
| XM_005259215.3 | 1768 | Intron | XP_005259272.1 | ||
| XM_011527278.2 | 1768 | Intron | XP_011525580.1 | ||
| XM_011527279.2 | 1768 | UTR 5 | XP_011525581.1 | ||
| XM_017027248.1 | 1768 | Intron | XP_016882737.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297588.1 | 1768 | Silent Mutation | ACA,ACG | T526T | NP_001284517.1 |
| NM_001297589.1 | 1768 | Silent Mutation | ACA,ACG | T526T | NP_001284518.1 |
| NM_013359.2 | 1768 | Silent Mutation | ACA,ACG | T526T | NP_037491.2 |
| XM_017027232.1 | 1768 | Intron | XP_016882721.1 | ||
| XM_017027233.1 | 1768 | Silent Mutation | ACA,ACG | T468T | XP_016882722.1 |