ENST00000394867.9:n.1150G>A
|
|
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ENST00000687128.1:n.1150G>A
|
|
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ENST00000688002.1:n.1005G>A
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|
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ENST00000689792.1:n.646-31G>A
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|
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ENST00000262948.10:c.711G>A
MANE Select
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ENSP00000262948.4:p.Glu237=
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ENST00000262948.9:c.711G>A
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ENSP00000262948.3:p.Glu237=
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|
ENST00000394867.8:c.420G>A
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ENSP00000378336.1:p.Glu140=
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|
ENST00000593364.5:n.658G>A
|
|
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ENST00000595715.1:n.526G>A
|
|
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ENST00000597263.5:n.169+1610G>A
|
|
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ENST00000599021.1:c.29+1610G>A
|
|
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ENST00000600584.5:n.1271G>A
|
|
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ENST00000601786.5:n.1012G>A
|
|
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ENST00000602167.5:n.431G>A
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|
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NM_030662.3:c.711G>A , LRG_750t1:c.711G>A
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NP_109587.1:p.Glu237=
|
|
XM_006722799.2:c.705+1610G>A
|
XP_006722862.1:n.705+1610G>A
|
|
XM_011528133.1:c.141G>A
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XP_011526435.1:p.Glu47=
|
|
XM_017026989.1:c.711G>A
|
XP_016882478.1:p.Glu237=
|
|
XM_017026990.1:c.705+1610G>A
|
XP_016882479.1:n.705+1610G>A
|
|
NM_030662.4:c.711G>A
MANE Select
|
NP_109587.1:p.Glu237=
|
|