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Homo sapiens egl-9 family hypoxia inducible factor 3 (EGLN3), transcript variant 2, mRNA

NCBI Reference Sequence: NM_001308103.2

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  • Run BLAST
    Find regions of similarity between this sequence and other sequences using BLAST.
  • Pick Primers
    Design and test primers for this sequence using Primer-BLAST.
  • Highlight Sequence Features
    Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
  • Find in this Sequence
    Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...
  • Show in Genome Data Viewer
    Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

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