Homo sapiens spectrin beta, erythrocytic (SPTB), transcript variant 3, - Nucleotide

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[Analysis of the characteristics of SPTB gene variants among 16 children with Hereditary spherocytosis]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Analysis of the characteristics of SPTB gene variants among 16 children with Hereditary spherocytosis].
Ge Y, Li J, Han Y, Xie H, Shangguan S, Jiang Q, Chen X, Liu R. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Mar 10; 40(3):269-275.
[Genetic Analysis of a Chinese Pedigree with Hereditary Spherocytosis Caused by Copy Number Variation Deletion of SPTB Gene]. [Zhongguo Shi Yan Xue Ye Xue Za...]
[Genetic Analysis of a Chinese Pedigree with Hereditary Spherocytosis Caused by Copy Number Variation Deletion of SPTB Gene].
Chen XL, Li JG, Men Q, Li X. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2023 Feb; 31(1):183-188.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. [Life Sci Alliance. 2022]
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Viard J, Loe-Mie Y, Daudin R, Khelfaoui M, Plancon C, Boland A, Tejedor F, Huganir RL, Kim E, Kinoshita M, et al. Life Sci Alliance. 2022 Aug 1; 5(12). Epub 2022 Aug 1.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the SPTB gene.
RefSeq protein product
See the reference protein sequence for spectrin beta chain, erythrocytic isoform a (NP_001020029.1).

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CDC42 cell division cycle 42 [Homo sapiens]
CDC42 cell division cycle 42 [Homo sapiens]
Gene ID:998

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Nucleotide