| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007039.3 | 3756 | Missense Mutation | ACG,AGG | T1144R | NP_008970.2 |
| XM_005267287.2 | 3756 | Missense Mutation | ACG,AGG | T1144R | XP_005267344.1 |
| XM_006720011.3 | 3756 | Missense Mutation | ACG,AGG | T1021R | XP_006720074.1 |
| XM_011536367.2 | 3756 | Missense Mutation | ACG,AGG | T1144R | XP_011534669.1 |
| XM_011536368.2 | 3756 | Missense Mutation | ACG,AGG | T1021R | XP_011534670.1 |
| XM_011536369.2 | 3756 | Missense Mutation | ACG,AGG | T940R | XP_011534671.1 |
| XM_017020938.1 | 3756 | Missense Mutation | ACG,AGG | T1021R | XP_016876427.1 |
| XM_017020939.1 | 3756 | Missense Mutation | ACG,AGG | T940R | XP_016876428.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040428.3 | 3756 | Intron | NP_001035518.1 | ||
| NM_018418.4 | 3756 | Intron | NP_060888.2 | ||
| XM_005267851.1 | 3756 | Intron | XP_005267908.1 | ||
| XM_005267852.1 | 3756 | Intron | XP_005267909.1 | ||
| XM_005267854.1 | 3756 | Intron | XP_005267911.1 | ||
| XM_005267855.1 | 3756 | Intron | XP_005267912.1 | ||
| XM_006720204.1 | 3756 | Intron | XP_006720267.1 | ||
| XM_006720205.1 | 3756 | Intron | XP_006720268.1 | ||
| XM_011536951.1 | 3756 | Intron | XP_011535253.1 | ||
| XM_011536952.1 | 3756 | Intron | XP_011535254.1 | ||
| XM_011536953.1 | 3756 | Intron | XP_011535255.1 | ||
| XM_017021452.1 | 3756 | Intron | XP_016876941.1 | ||
| XM_017021453.1 | 3756 | Intron | XP_016876942.1 | ||
| XM_017021454.1 | 3756 | Intron | XP_016876943.1 | ||
| XM_017021455.1 | 3756 | Intron | XP_016876944.1 | ||
| XM_017021456.1 | 3756 | Intron | XP_016876945.1 | ||
| XM_017021457.1 | 3756 | Intron | XP_016876946.1 |