| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281437.1 | 11000 | Intron | NP_001268366.1 | ||
| NM_001281438.1 | 11000 | Intron | NP_001268367.1 | ||
| NM_007002.3 | 11000 | Intron | NP_008933.2 | ||
| NM_175573.2 | 11000 | Intron | NP_783163.1 | ||
| XM_005260257.1 | 11000 | Intron | XP_005260314.1 | ||
| XM_011528503.1 | 11000 | Intron | XP_011526805.1 | ||
| XM_017027602.1 | 11000 | Intron | XP_016883091.1 | ||
| XM_017027603.1 | 11000 | Intron | XP_016883092.1 | ||
| XM_017027604.1 | 11000 | Intron | XP_016883093.1 | ||
| XM_017027605.1 | 11000 | Intron | XP_016883094.1 | ||
| XM_017027606.1 | 11000 | Intron | XP_016883095.1 | ||
| XM_017027607.1 | 11000 | Intron | XP_016883096.1 | ||
| XM_017027608.1 | 11000 | Intron | XP_016883097.1 | ||
| XM_017027609.1 | 11000 | Intron | XP_016883098.1 | ||
| XM_017027610.1 | 11000 | Intron | XP_016883099.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005560.4 | 11000 | Missense Mutation | CGG,TGG | R3685W | NP_005551.3 |
| XM_006723796.3 | 11000 | Missense Mutation | CGG,TGG | R3690W | XP_006723859.1 |
| XM_006723798.3 | 11000 | Intron | XP_006723861.1 | ||
| XM_011528818.2 | 11000 | Missense Mutation | CGG,TGG | R3644W | XP_011527120.1 |
| XM_011528819.2 | 11000 | Missense Mutation | CGG,TGG | R3599W | XP_011527121.1 |