ENST00000422447.8:c.993A>T
MANE Select
|
ENSP00000395337.3:p.Gln331His
|
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ENST00000227157.8:c.*143A>T
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ENSP00000227157.4:n.*143A>T
|
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ENST00000375710.7:n.1860A>T
|
|
|
ENST00000379412.9:c.993A>T
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ENSP00000368722.5:p.Gln331His
|
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ENST00000396222.6:c.724A>T
|
ENSP00000379524.2:p.Ile242Phe
|
|
ENST00000422447.7:c.993A>T
|
ENSP00000395337.3:p.Gln331His
|
|
ENST00000430553.6:c.819A>T
|
ENSP00000406172.2:p.Gln273His
|
|
ENST00000538451.1:n.880A>T
|
|
|
ENST00000540430.5:c.1080A>T
|
ENSP00000445175.1:p.Gln360His
|
|
ENST00000542179.1:c.993A>T
|
ENSP00000445331.1:p.Gln331His
|
|
ENST00000545215.5:c.*737A>T
|
ENSP00000442637.1:n.*737A>T
|
|
NM_001135239.1:c.819A>T
|
NP_001128711.1:p.Gln273His
|
|
NM_001165414.1:c.1080A>T
|
NP_001158886.1:p.Gln360His
|
|
NM_001165415.1:c.724A>T
|
NP_001158887.1:p.Ile242Phe
|
|
NM_001165416.1:c.*143A>T
|
NP_001158888.1:n.*143A>T
|
|
NM_005566.3:c.993A>T
|
NP_005557.1:p.Gln331His
|
|
NR_028500.1:n.1147A>T
|
|
|
NM_005566.4:c.993A>T
MANE Select
|
NP_005557.1:p.Gln331His
|
|
NM_001165415.2:c.724A>T
|
NP_001158887.1:p.Ile242Phe
|
|
NM_001135239.2:c.819A>T
|
NP_001128711.1:p.Gln273His
|
|
NM_001165414.2:c.1080A>T
|
NP_001158886.1:p.Gln360His
|
|
NM_001165416.2:c.*143A>T
|
NP_001158888.1:n.*143A>T
|
|
NR_028500.2:n.973A>T
|
|
|