| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007218.3 | 774 | Intron | NP_009149.2 | ||
| XM_017013002.1 | 774 | Intron | XP_016868491.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146160.1 | 774 | Missense Mutation | AAT,AGT | N236S | NP_001139632.1 |
| NM_001317889.1 | 774 | Missense Mutation | AAT,AGT | N319S | NP_001304818.1 |
| NM_001317890.1 | 774 | Missense Mutation | AAT,AGT | N229S | NP_001304819.1 |
| NM_001317891.1 | 774 | Missense Mutation | AAT,AGT | N138S | NP_001304820.1 |
| NM_032026.3 | 774 | Missense Mutation | AAT,AGT | N283S | NP_114415.1 |
| XM_006716666.3 | 774 | Intron | XP_006716729.1 | ||
| XM_006716667.3 | 774 | Intron | XP_006716730.1 | ||
| XM_006716668.3 | 774 | Intron | XP_006716731.1 | ||
| XM_006716669.3 | 774 | Intron | XP_006716732.1 | ||
| XM_006716670.3 | 774 | Intron | XP_006716733.1 | ||
| XM_006716671.3 | 774 | Intron | XP_006716734.1 | ||
| XM_011517331.2 | 774 | Intron | XP_011515633.1 | ||
| XM_017013895.1 | 774 | Intron | XP_016869384.1 | ||
| XM_017013896.1 | 774 | Intron | XP_016869385.1 | ||
| XM_017013897.1 | 774 | Intron | XP_016869386.1 | ||
| XM_017013898.1 | 774 | Intron | XP_016869387.1 | ||
| XM_017013899.1 | 774 | Intron | XP_016869388.1 |