ENST00000588860.6:c.1164G>T
|
ENSP00000465878.2:p.Gln388His
|
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ENST00000589076.6:c.1164G>T
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ENSP00000466934.2:p.Gln388His
|
|
ENST00000589941.2:c.1164G>T
|
ENSP00000465874.2:p.Gln388His
|
|
ENST00000590061.2:c.1164G>T
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ENSP00000464772.2:p.Gln388His
|
|
ENST00000593223.2:c.1164G>T
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ENSP00000466118.2:p.Gln388His
|
|
ENST00000611848.2:c.1164G>T
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ENSP00000478613.2:p.Gln388His
|
|
ENST00000684953.1:n.2536G>T
|
|
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ENST00000685090.1:n.1615G>T
|
|
|
ENST00000685232.1:n.1272G>T
|
|
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ENST00000688574.1:n.1272G>T
|
|
|
ENST00000691124.1:n.2646G>T
|
|
|
ENST00000342988.8:c.1164G>T
MANE Select
|
ENSP00000341551.3:p.Gln388His
|
|
ENST00000342988.7:c.1164G>T
|
ENSP00000341551.3:p.Gln388His
|
|
ENST00000398417.6:c.1164G>T
|
ENSP00000381452.1:p.Gln388His
|
|
ENST00000588745.5:c.876G>T
|
ENSP00000464901.1:p.Gln292His
|
|
ENST00000590499.1:n.222G>T
|
|
|
ENST00000591126.5:n.3165G>T
|
|
|
ENST00000592186.5:c.955+7127G>T
|
ENSP00000468611.1:n.955+7127G>T
|
|
ENST00000611848.1:c.364G>T
|
|
|
NM_005359.5:c.1164G>T , LRG_318t1:c.1164G>T
|
NP_005350.1:p.Gln388His
|
|
NM_005359.6:c.1164G>T
MANE Select
|
NP_005350.1:p.Gln388His
|
|