Homo sapiens SEC14 like lipid binding 4 (SEC14L4), transcript variant - Nucleotide

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Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes. [Proc Natl Acad Sci U S A. 2020]
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes.
Rausell A, Luo Y, Lopez M, Seeleuthner Y, Rapaport F, Favier A, Stenson PD, Cooper DN, Patin E, Casanova JL, et al. Proc Natl Acad Sci U S A. 2020 Jun 16; 117(24):13626-13636. Epub 2020 Jun 2.
The mutational constraint spectrum quantified from variation in 141,456 humans. [Nature. 2020]
The mutational constraint spectrum quantified from variation in 141,456 humans.
Karczewski KJ, Francioli LC, Tiao G, Cummings BB, Alföldi J, Wang Q, Collins RL, Laricchia KM, Ganna A, Birnbaum DP, et al. Nature. 2020 May; 581(7809):434-443. Epub 2020 May 27.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the SEC14L4 gene (NM_001161368.3).
RefSeq protein product
See the reference protein sequence for SEC14-like protein 4 isoform a (NP_777637.1).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide