ENST00000394867.9:n.1566A>T
|
|
|
ENST00000688002.1:n.3278A>T
|
|
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ENST00000688751.1:n.263A>T
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|
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ENST00000689792.1:n.1031A>T
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|
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ENST00000262948.10:c.1127A>T
MANE Select
|
ENSP00000262948.4:p.Glu376Val
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|
ENST00000262948.9:c.1127A>T
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ENSP00000262948.3:p.Glu376Val
|
|
ENST00000394867.8:c.836A>T
|
ENSP00000378336.1:p.Glu279Val
|
|
ENST00000597263.5:n.312A>T
|
|
|
ENST00000599021.1:c.237A>T
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|
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ENST00000600584.5:n.2576A>T
|
|
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ENST00000601786.5:n.1428A>T
|
|
|
NM_030662.3:c.1127A>T , LRG_750t1:c.1127A>T
|
NP_109587.1:p.Glu376Val
|
|
XM_006722799.2:c.848A>T
|
XP_006722862.1:p.Glu283Val
|
|
XM_011528133.1:c.557A>T
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XP_011526435.1:p.Glu186Val
|
|
NM_030662.4:c.1127A>T
MANE Select
|
NP_109587.1:p.Glu376Val
|
|