ENST00000394867.9:n.1567A>G
|
|
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ENST00000688002.1:n.3279A>G
|
|
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ENST00000688751.1:n.264A>G
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|
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ENST00000689792.1:n.1032A>G
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|
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ENST00000262948.10:c.1128A>G
MANE Select
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ENSP00000262948.4:p.Glu376=
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ENST00000262948.9:c.1128A>G
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ENSP00000262948.3:p.Glu376=
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ENST00000394867.8:c.837A>G
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ENSP00000378336.1:p.Glu279=
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ENST00000597263.5:n.313A>G
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|
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ENST00000599021.1:c.238A>G
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ENST00000600584.5:n.2577A>G
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|
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ENST00000601786.5:n.1429A>G
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NM_030662.3:c.1128A>G , LRG_750t1:c.1128A>G
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NP_109587.1:p.Glu376=
|
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XM_006722799.2:c.849A>G
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XP_006722862.1:p.Glu283=
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XM_011528133.1:c.558A>G
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XP_011526435.1:p.Glu186=
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|
NM_030662.4:c.1128A>G
MANE Select
|
NP_109587.1:p.Glu376=
|
|