ENST00000413384.7:c.177G>A
MANE Select
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ENSP00000405600.2:p.Gly59=
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ENST00000677246.1:c.177G>A
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ENSP00000504447.1:p.Gly59=
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ENST00000310317.9:c.52-278G>A
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ENSP00000311402.5:n.52-278G>A
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ENST00000392826.6:c.150G>A
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ENSP00000376571.2:p.Gly50=
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ENST00000413384.6:c.177G>A
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ENSP00000405600.2:p.Gly59=
|
|
ENST00000461735.1:c.135G>A
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ENSP00000419164.1:p.Gly45=
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ENST00000463414.5:c.177G>A
|
ENSP00000418584.1:p.Gly59=
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ENST00000482950.5:c.177G>A
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ENSP00000419379.1:p.Gly59=
|
|
ENST00000483786.5:c.177G>A
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ENSP00000417808.1:p.Gly59=
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|
ENST00000485713.5:c.177G>A
|
ENSP00000419412.1:p.Gly59=
|
|
ENST00000488420.1:c.177G>A
|
ENSP00000417221.1:p.Gly59=
|
|
ENST00000490898.5:c.177G>A
|
ENSP00000418114.1:p.Gly59=
|
|
ENST00000494125.1:n.412G>A
|
|
|
NM_001199692.1:c.177G>A
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NP_001186621.1:p.Gly59=
|
|
NM_001199693.1:c.150G>A
|
NP_001186622.1:p.Gly50=
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|
NM_001199694.1:c.135G>A
|
NP_001186623.1:p.Gly45=
|
|
NM_003040.3:c.177G>A
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NP_003031.3:p.Gly59=
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XM_006716094.2:c.177G>A
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XP_006716157.1:p.Gly59=
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XM_011516497.1:c.177G>A
|
XP_011514799.1:p.Gly59=
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NM_001199692.2:c.177G>A
|
NP_001186621.1:p.Gly59=
|
|
NM_001199694.2:c.135G>A
|
NP_001186623.1:p.Gly45=
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XM_006716094.3:c.177G>A
|
XP_006716157.1:p.Gly59=
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|
NM_003040.4:c.177G>A
MANE Select
|
NP_003031.3:p.Gly59=
|
|
NM_001199692.3:c.177G>A
|
NP_001186621.1:p.Gly59=
|
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