ENST00000461280.2:n.1050C>A
|
|
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ENST00000684241.1:n.2585C>A
|
|
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ENST00000262186.10:c.1752C>A
MANE Select
|
ENSP00000262186.5:p.Gly584=
|
|
ENST00000330883.9:c.732C>A
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ENSP00000328531.4:p.Gly244=
|
|
ENST00000262186.9:c.1752C>A
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ENSP00000262186.5:p.Gly584=
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|
ENST00000330883.8:c.732C>A
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ENSP00000328531.4:p.Gly244=
|
|
ENST00000430723.4:c.1404C>A
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ENSP00000387657.4:p.Gly468=
|
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ENST00000461280.1:n.1039C>A
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ENST00000473610.5:n.1057C>A
|
|
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ENST00000532957.5:n.1975C>A
|
|
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NM_000238.3:c.1752C>A , LRG_288t1:c.1752C>A
|
NP_000229.1:p.Gly584=
|
|
NM_001204798.1:c.732C>A
|
NP_001191727.1:p.Gly244=
|
|
NM_172056.2:c.1752C>A , LRG_288t2:c.1752C>A
|
NP_742053.1:p.Gly584=
|
|
NM_172057.2:c.732C>A , LRG_288t3:c.732C>A
|
NP_742054.1:p.Gly244=
|
|
XM_011516185.1:c.1452C>A
|
XP_011514487.1:p.Gly484=
|
|
XM_011516186.1:c.1752C>A
|
XP_011514488.1:p.Gly584=
|
|
XM_011516185.2:c.1452C>A
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XP_011514487.1:p.Gly484=
|
|
XM_011516186.3:c.1752C>A
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XP_011514488.1:p.Gly584=
|
|
XM_017012195.1:c.1602C>A
|
XP_016867684.1:p.Gly534=
|
|
XM_017012196.1:c.1575C>A
|
XP_016867685.1:p.Gly525=
|
|
NM_000238.4:c.1752C>A
MANE Select
|
NP_000229.1:p.Gly584=
|
|
NM_001204798.2:c.732C>A
|
NP_001191727.1:p.Gly244=
|
|
NM_172057.3:c.732C>A
|
NP_742054.1:p.Gly244=
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