ENST00000394867.9:n.1154T>G
|
|
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ENST00000687128.1:n.1154T>G
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|
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ENST00000688002.1:n.1009T>G
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|
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ENST00000689792.1:n.646-27T>G
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|
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ENST00000262948.10:c.715T>G
MANE Select
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ENSP00000262948.4:p.Leu239Val
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ENST00000262948.9:c.715T>G
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ENSP00000262948.3:p.Leu239Val
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|
ENST00000394867.8:c.424T>G
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ENSP00000378336.1:p.Leu142Val
|
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ENST00000593364.5:n.662T>G
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|
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ENST00000595715.1:n.530T>G
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|
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ENST00000597263.5:n.169+1614T>G
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|
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ENST00000599021.1:c.29+1614T>G
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|
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ENST00000600584.5:n.1275T>G
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|
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ENST00000601786.5:n.1016T>G
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|
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NM_030662.3:c.715T>G , LRG_750t1:c.715T>G
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NP_109587.1:p.Leu239Val
|
|
XM_006722799.2:c.705+1614T>G
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XP_006722862.1:n.705+1614T>G
|
|
XM_011528133.1:c.145T>G
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XP_011526435.1:p.Leu49Val
|
|
XM_017026989.1:c.715T>G
|
XP_016882478.1:p.Leu239Val
|
|
XM_017026990.1:c.705+1614T>G
|
XP_016882479.1:n.705+1614T>G
|
|
NM_030662.4:c.715T>G
MANE Select
|
NP_109587.1:p.Leu239Val
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