| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_173525.2 | 2951 | Intron | NP_775796.2 | ||
| XM_011519926.2 | 2951 | Intron | XP_011518228.1 | ||
| XM_011519927.2 | 2951 | Intron | XP_011518229.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098794.1 | 2951 | Missense Mutation | ACC,GCC | T872A | NP_001092264.1 |
| NM_032127.3 | 2951 | Missense Mutation | ACC,GCC | T886A | NP_115503.2 |
| XM_006718343.2 | 2951 | Missense Mutation | ACC,GCC | T886A | XP_006718406.1 |
| XM_011520397.2 | 2951 | Missense Mutation | ACC,GCC | T886A | XP_011518699.1 |
| XM_011520398.2 | 2951 | Intron | XP_011518700.1 | ||
| XM_011520399.2 | 2951 | Intron | XP_011518701.1 |