| exon_id | ENSE00001212207, ENSE00003479884, ENSE00003653874, ENSE00003502583, ENSE00003556024, ENSE00003675075, ENSE00001447358, ENSE00001447359 |
| disease_description | Hepatocarcinogenesis,Congenital Abnormality,Neuroectodermal Tumor, Primitive,Tumor Progression,Diffuse Large B-Cell Lymphoma,Paresis,Malignant neoplasm of thyroid,Extraosseous Ewings sarcoma-primitive neuroepithelial tumor,Malignant neoplasm of liver,Myopathies, Nemaline,Ki-1+ Anaplastic Large Cell Lymphoma,Liver and Intrahepatic Biliary Tract Carcinoma,Colorectal cancer metastatic,Inflammatory Myofibroblastic Tumor,Embryonal Neoplasm,Mammary Neoplasms, Experimental,Retinoblastoma,Mastocytosis,Myopathy,Stomach Neoplasms,Lymphoma, Large-Cell, Follicular,Papillary thyroid carcinoma,Anaplastic Large Cell Lymphoma, ALK-Positive,Neuroblastoma,Urticaria Pigmentosa,Cervix carcinoma,Nemaline Myopathy, Autosomal Dominant,Choriocarcinoma,Cap Myopathy,Autosomal dominant retinitis pigmentosa,Nemaline Myopathy, Autosomal Recessive,Nemaline myopathy 1,Lymphoma,Congenital myopathy (disorder),Congenital Fiber Type Disproportion,Hypertrophic Cardiomyopathy,Ileocolic intussusception,Thyroid carcinoma,Ce |