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NR_168082.1 - -
NR_168078.1 - -
NR_168083.1 - -
NR_168079.1 - -
NR_168076.1 - -
NR_168080.1 - -
NR_168081.1 - -
NR_168084.1 - -
NR_168077.1 - -
NM_001382333.1 - NP_001369262.1
NM_001382328.1 - NP_001369257.1
NM_001382331.1 - NP_001369260.1
NM_001382324.1 - NP_001369253.1
NM_001382323.2 - NP_001369252.1 (MANE)
NM_001382339.1 - NP_001369268.1
NM_001382341.1 - NP_001369270.1
NM_001382334.1 - NP_001369263.1
NM_001382332.1 - NP_001369261.1
NM_001382336.1 - NP_001369265.1
NM_001382325.1 - NP_001369254.1
NM_001382329.1 - NP_001369258.1
NM_001382338.1 - NP_001369267.1
NM_001382326.1 - NP_001369255.1
NM_001382327.1 - NP_001369256.1
NM_001382335.1 - NP_001369264.1
NM_001382340.1 - NP_001369269.1
NM_001382330.1 - NP_001369259.1
NM_001382337.1 - NP_001369266.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
11
Location
Chr11:125,164,251-125,433,889
LOEUF
0.272
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Pathogenic/ Likely pa...
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ToMMo
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By consequences
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Gene region:
CDS
SpliceSite
UTR
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External resources
PKNOX2
PBX/knotted 1 homeobox 2
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Variant Map
DNA Sequence
Variant Map
Amino Acid Sequence
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