Homo sapiens soluble FGFR2 variant 2 (FGFR2) mRNA, complete cds, alter - Nucleotide

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Genetic insights into the 'sandwich fusion' subtype of Klippel-Feil syndrome: novel FGFR2 mutations identified by 21 cases of whole-exome sequencing. [Orphanet J Rare Dis. 2024]
Genetic insights into the 'sandwich fusion' subtype of Klippel-Feil syndrome: novel FGFR2 mutations identified by 21 cases of whole-exome sequencing.
Xu N, Hung KL, Gong X, Fan D, Tian Y, Yan M, Wei Y, Wang S. Orphanet J Rare Dis. 2024 Apr 1; 19(1):141. Epub 2024 Apr 1.
Superficial acral calcified chondroid mesenchymal neoplasm harboring an FN1::FGFR2 fusion and review of the literature. [J Cutan Pathol. 2024]
Superficial acral calcified chondroid mesenchymal neoplasm harboring an FN1::FGFR2 fusion and review of the literature.
Machado I, Damaskou V, Ioannidis E, Jour G, Linos K. J Cutan Pathol. 2024 May; 51(5):338-344. Epub 2024 Feb 8.
Investigating FGFR2 gene as a blood-based epigenetic biomarker in gastric cancer. [Mol Biol Rep. 2024]
Investigating FGFR2 gene as a blood-based epigenetic biomarker in gastric cancer.
Aleyasin SA, Moradi A, Abolhasani N, Abdollahi M. Mol Biol Rep. 2024 Feb 1; 51(1):253. Epub 2024 Feb 1.

RefSeq alternative splicing
See 34 reference mRNA sequence splice variants for the FGFR2 gene.

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Nucleotide