ENST00000209873.9:c.987G>T
MANE Select
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ENSP00000209873.4:p.Gly329=
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ENST00000546393.7:n.1832G>T
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ENST00000546562.6:n.2051G>T
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ENST00000547238.6:n.1623G>T
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ENST00000547520.6:n.981G>T
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ENST00000547757.2:c.36G>T
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ENSP00000448020.2:p.Gly12=
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ENST00000548880.2:n.1437G>T
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ENST00000548931.6:c.507G>T
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ENSP00000457518.1:p.Gly169=
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ENST00000549450.6:n.921G>T
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ENST00000552161.6:n.1943G>T
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ENST00000672797.1:n.1440G>T
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ENST00000672900.1:n.1785G>T
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ENST00000209873.8:c.987G>T
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ENSP00000209873.4:p.Gly329=
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ENST00000394384.7:c.888G>T
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ENSP00000377908.3:p.Gly296=
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ENST00000546572.1:n.575G>T
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ENST00000547520.5:n.691G>T
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ENST00000548931.5:c.507G>T
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ENSP00000457518.1:p.Gly169=
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ENST00000550033.5:n.242G>T
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ENST00000550286.5:c.615G>T
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ENSP00000446885.1:p.Gly205=
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ENST00000552876.5:n.1330G>T
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NM_001173466.1:c.888G>T
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NP_001166937.1:p.Gly296=
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NM_015665.5:c.987G>T
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NP_056480.1:p.Gly329=
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XM_006719617.2:c.1002G>T
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XP_006719680.1:p.Gly334=
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XM_006719619.2:c.1002G>T
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XP_006719682.1:p.Gly334=
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XM_011538777.1:c.1002G>T
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XP_011537079.1:p.Gly334=
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XM_011538778.1:c.987G>T
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XP_011537080.1:p.Gly329=
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XM_011538779.1:c.903G>T
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XP_011537081.1:p.Gly301=
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XM_011538780.1:c.888G>T
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XP_011537082.1:p.Gly296=
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XM_011538781.1:c.336G>T
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XP_011537083.1:p.Gly112=
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XM_011538778.2:c.987G>T
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XP_011537080.1:p.Gly329=
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XM_011538780.2:c.888G>T
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XP_011537082.1:p.Gly296=
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XR_001748875.2:n.1008G>T
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NM_015665.6:c.987G>T
MANE Select
|
NP_056480.1:p.Gly329=
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NM_001173466.2:c.888G>T
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NP_001166937.1:p.Gly296=
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