Homo sapiens AKT serine/threonine kinase 3 (AKT3), transcript variant - Nucleotide

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A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids. [Biochim Biophys Acta Mol Basis...]
A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids.
Xu Y, Lu R, Li H, Feng W, Zhao R. Biochim Biophys Acta Mol Basis Dis. 2024 Aug; 1870(6):167232. Epub 2024 May 15.
Differential prognostic values of the three AKT isoforms in acute myeloid leukemia. [Sci Rep. 2024]
Differential prognostic values of the three AKT isoforms in acute myeloid leukemia.
Corre E, Soum C, Pfeifer R, Bessière C, Dailhau S, Marbœuf C, Meggetto F, Touriol C, Récher C, Bousquet M, et al. Sci Rep. 2024 Mar 25; 14(1):7070. Epub 2024 Mar 25.
Autocrine Regulation of Interleukin-6 via the Activation of STAT3 and Akt in Cardiac Myxoma Cells. [Int J Mol Sci. 2024]
Autocrine Regulation of Interleukin-6 via the Activation of STAT3 and Akt in Cardiac Myxoma Cells.
Jougasaki M, Takenoshita Y, Umebashi K, Yamamoto M, Sudou K, Nakashima H, Sonoda M, Kinjo T. Int J Mol Sci. 2024 Feb 13; 25(4). Epub 2024 Feb 13.

RefSeq alternative splicing
See 29 reference mRNA sequence splice variants for the AKT3 gene.

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Protein sequence from Nucleotide coding region
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Nucleotide