Homo sapiens CF transmembrane conductance regulator (CFTR), mRNA

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Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations. [Mol Biol Rep. 2024]
Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations.
Waheed N, Waris R, Naseer M, Razzaq A, Haider N, Shah AA, Ullah A. Mol Biol Rep. 2024 Apr 25; 51(1):573. Epub 2024 Apr 25.
Functional Consequences of CFTR Interactions in Cystic Fibrosis. [Int J Mol Sci. 2024]
Functional Consequences of CFTR Interactions in Cystic Fibrosis.
Ramananda Y, Naren AP, Arora K. Int J Mol Sci. 2024 Mar 16; 25(6). Epub 2024 Mar 16.
CFTR function is impaired in a subset of patients with pancreatitis carrying rare CFTR variants. [Pancreatology. 2024]
CFTR function is impaired in a subset of patients with pancreatitis carrying rare CFTR variants.
Angyal D, Kleinfelder K, Ciciriello F, Groeneweg TA, De Marchi G, de Pretis N, Bernardoni L, Rodella L, Tomba F, De Angelis P, et al. Pancreatology. 2024 May; 24(3):394-403. Epub 2024 Mar 10.

RefSeq protein product
See the reference protein sequence for cystic fibrosis transmembrane conductance regulator (NP_000483.3).

Protein
Protein sequence from Nucleotide coding region
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centriolar satellite-associated tubulin polyglutamylase complex regulator 1 isof...
centriolar satellite-associated tubulin polyglutamylase complex regulator 1 isoform 1 [Homo sapiens]
gi|51558745|ref|NP_001003676.1|

Protein

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Nucleotide