ENST00000455537.7:c.1176G>A
MANE Select
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ENSP00000408979.2:p.Glu392=
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ENST00000674619.1:c.1176G>A
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ENSP00000502270.1:p.Glu392=
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ENST00000675882.1:n.163G>A
|
|
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ENST00000676081.1:n.322G>A
|
|
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ENST00000676457.1:c.1071G>A
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ENSP00000501588.1:p.Glu357=
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ENST00000286452.5:c.909G>A
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ENSP00000286452.5:p.Glu303=
|
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ENST00000455537.6:c.1176G>A
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ENSP00000408979.2:p.Glu392=
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NM_004984.2:c.1176G>A
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NP_004975.2:p.Glu392=
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NM_001354705.1:c.909G>A
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NP_001341634.1:p.Glu303=
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NM_004984.3:c.1176G>A
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NP_004975.2:p.Glu392=
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XR_002957324.1:n.1409G>A
|
|
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NM_004984.4:c.1176G>A
MANE Select
|
NP_004975.2:p.Glu392=
|
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NM_001354705.2:c.909G>A
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NP_001341634.1:p.Glu303=
|
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