| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001161415.1 | 775 | Missense Mutation | ACG,ATG | T55M | NP_001154887.1 |
| NM_001161416.1 | 775 | Missense Mutation | ACG,ATG | T27M | NP_001154888.1 |
| NM_001161417.1 | 775 | Missense Mutation | ACG,ATG | T27M | NP_001154889.1 |
| NM_005291.2 | 775 | Missense Mutation | ACG,ATG | T55M | NP_005282.1 |
| XM_017003833.1 | 775 | Missense Mutation | ACG,ATG | T55M | XP_016859322.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136037.2 | 775 | Intron | NP_001129509.2 | ||
| NM_001161403.1 | 775 | Intron | NP_001154875.1 | ||
| NM_001161404.1 | 775 | Intron | NP_001154876.1 | ||
| NM_001256542.1 | 775 | Intron | NP_001243471.1 | ||
| NM_017980.4 | 775 | Intron | NP_060450.2 | ||
| XM_005263710.2 | 775 | Intron | XP_005263767.1 | ||
| XM_006712627.3 | 775 | Intron | XP_006712690.1 | ||
| XM_006712628.3 | 775 | Intron | XP_006712691.1 | ||
| XM_011511453.1 | 775 | Intron | XP_011509755.1 | ||
| XM_017004469.1 | 775 | Intron | XP_016859958.1 |