| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003757.3 | 569 | Silent Mutation | TCC,TCG | S12S | NP_003748.1 |
| XM_017002671.1 | 569 | UTR 5 | XP_016858160.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019118.4 | 569 | Intron | NP_061991.3 | ||
| XM_011541795.2 | 569 | Intron | XP_011540097.1 | ||
| XM_017001812.1 | 569 | Intron | XP_016857301.1 | ||
| XM_017001813.1 | 569 | Intron | XP_016857302.1 | ||
| XM_017001814.1 | 569 | Intron | XP_016857303.1 | ||
| XM_017001815.1 | 569 | Intron | XP_016857304.1 | ||
| XM_017001816.1 | 569 | Intron | XP_016857305.1 | ||
| XM_017001817.1 | 569 | Intron | XP_016857306.1 | ||
| XM_017001818.1 | 569 | Intron | XP_016857307.1 | ||
| XM_017001819.1 | 569 | Intron | XP_016857308.1 | ||
| XM_017001820.1 | 569 | Intron | XP_016857309.1 | ||
| XM_017001821.1 | 569 | Intron | XP_016857310.1 | ||
| XM_017001822.1 | 569 | Intron | XP_016857311.1 | ||
| XM_017001823.1 | 569 | Intron | XP_016857312.1 | ||
| XM_017001824.1 | 569 | Intron | XP_016857313.1 | ||
| XM_017001825.1 | 569 | Intron | XP_016857314.1 | ||
| XM_017001826.1 | 569 | Intron | XP_016857315.1 | ||
| XM_017001827.1 | 569 | Intron | XP_016857316.1 | ||
| XM_017001828.1 | 569 | Intron | XP_016857317.1 | ||
| XM_017001829.1 | 569 | Intron | XP_016857318.1 | ||
| XM_017001830.1 | 569 | Intron | XP_016857319.1 | ||
| XM_017001831.1 | 569 | Intron | XP_016857320.1 |