ENST00000354674.5:c.1529A>T
MANE Plus Clinical
|
ENSP00000346701.4:p.Glu510Val
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ENST00000367255.10:c.24995A>T
MANE Select
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ENSP00000356224.5:p.Glu8332Val
|
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ENST00000423061.6:c.24851A>T
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ENSP00000396024.1:p.Glu8284Val
|
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ENST00000672154.1:c.397A>T
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|
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ENST00000672169.1:c.730A>T
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|
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ENST00000673173.1:c.891-3586A>T
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|
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ENST00000673451.1:c.767A>T
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ENSP00000500189.1:p.Glu256Val
|
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ENST00000341594.9:c.23780A>T
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ENSP00000341887.6:p.Glu7927Val
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ENST00000347037.9:n.1743A>T
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|
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ENST00000354674.4:c.1529A>T
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ENSP00000346701.4:p.Glu510Val
|
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ENST00000367251.7:c.3830A>T
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ENSP00000356220.3:p.Glu1277Val
|
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ENST00000367255.9:c.24995A>T
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ENSP00000356224.5:p.Glu8332Val
|
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ENST00000367256.9:n.8687A>T
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|
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ENST00000367257.8:c.2933A>T
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ENSP00000356226.4:p.Glu978Val
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ENST00000409694.6:n.8579A>T
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|
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ENST00000423061.5:c.24851A>T
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ENSP00000396024.1:p.Glu8284Val
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ENST00000460912.6:n.1609A>T
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ENST00000478916.5:n.4017A>T
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ENST00000536990.5:n.1832A>T
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|
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ENST00000539504.5:c.1460A>T
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ENSP00000441052.1:p.Glu487Val
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NM_033071.3:c.24851A>T
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NP_149062.1:p.Glu8284Val
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NM_182961.3:c.24995A>T
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NP_892006.3:p.Glu8332Val
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XM_006715407.1:c.25100A>T
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XP_006715470.1:p.Glu8367Val
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XM_006715408.1:c.25088A>T
|
XP_006715471.1:p.Glu8363Val
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|
XM_006715409.1:c.25079A>T
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XP_006715472.1:p.Glu8360Val
|
|
XM_006715410.1:c.25100A>T
|
XP_006715473.1:p.Glu8367Val
|
|
XM_006715411.1:c.25049A>T
|
XP_006715474.1:p.Glu8350Val
|
|
XM_006715412.1:c.25085A>T
|
XP_006715475.1:p.Glu8362Val
|
|
XM_006715413.1:c.25031A>T
|
XP_006715476.1:p.Glu8344Val
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|
XM_006715414.1:c.25028A>T
|
XP_006715477.1:p.Glu8343Val
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|
XM_006715415.1:c.25031A>T
|
XP_006715478.1:p.Glu8344Val
|
|
XM_006715416.1:c.25016A>T
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XP_006715479.1:p.Glu8339Val
|
|
XM_006715417.1:c.24959A>T
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XP_006715480.1:p.Glu8320Val
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XM_006715420.1:c.24947A>T
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XP_006715483.1:p.Glu8316Val
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XM_006715421.1:c.24944A>T
|
XP_006715484.1:p.Glu8315Val
|
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XM_006715422.1:c.24941A>T
|
XP_006715485.1:p.Glu8314Val
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XM_006715423.1:c.25100A>T
|
XP_006715486.1:p.Glu8367Val
|
|
XM_006715424.1:c.25100A>T
|
XP_006715487.1:p.Glu8367Val
|
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XM_006715425.1:c.25031A>T
|
XP_006715488.1:p.Glu8344Val
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XM_011535641.1:c.25097A>T
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XP_011533943.1:p.Glu8366Val
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XM_011535642.1:c.25085A>T
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XP_011533944.1:p.Glu8362Val
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|
XM_011535643.1:c.24935A>T
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XP_011533945.1:p.Glu8312Val
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XM_011535644.1:c.23375A>T
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XP_011533946.1:p.Glu7792Val
|
|
XM_011535645.1:c.22868A>T
|
XP_011533947.1:p.Glu7623Val
|
|
XM_011535647.1:c.18335A>T
|
XP_011533949.1:p.Glu6112Val
|
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NM_001347701.1:c.1601A>T
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NP_001334630.1:p.Glu534Val
|
|
NM_001347702.1:c.1529A>T
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NP_001334631.1:p.Glu510Val
|
|
XM_006715408.2:c.25088A>T
|
XP_006715471.1:p.Glu8363Val
|
|
XM_006715410.2:c.25100A>T
|
XP_006715473.1:p.Glu8367Val
|
|
XM_006715412.2:c.25085A>T
|
XP_006715475.1:p.Glu8362Val
|
|
XM_006715413.2:c.25031A>T
|
XP_006715476.1:p.Glu8344Val
|
|
XM_006715415.2:c.25031A>T
|
XP_006715478.1:p.Glu8344Val
|
|
XM_006715416.2:c.25016A>T
|
XP_006715479.1:p.Glu8339Val
|
|
XM_006715417.2:c.24959A>T
|
XP_006715480.1:p.Glu8320Val
|
|
XM_006715420.2:c.24947A>T
|
XP_006715483.1:p.Glu8316Val
|
|
XM_006715421.2:c.24944A>T
|
XP_006715484.1:p.Glu8315Val
|
|
XM_006715423.2:c.25100A>T
|
XP_006715486.1:p.Glu8367Val
|
|
XM_006715424.2:c.25100A>T
|
XP_006715487.1:p.Glu8367Val
|
|
XM_006715425.2:c.25031A>T
|
XP_006715488.1:p.Glu8344Val
|
|
XM_011535641.2:c.25097A>T
|
XP_011533943.1:p.Glu8366Val
|
|
XM_011535642.2:c.25085A>T
|
XP_011533944.1:p.Glu8362Val
|
|
XM_011535645.2:c.22868A>T
|
XP_011533947.1:p.Glu7623Val
|
|
XM_017010608.1:c.25100A>T
|
XP_016866097.1:p.Glu8367Val
|
|
XM_017010609.1:c.25100A>T
|
XP_016866098.1:p.Glu8367Val
|
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XM_017010610.1:c.25079A>T
|
XP_016866099.1:p.Glu8360Val
|
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XM_017010611.2:c.25073A>T
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XP_016866100.1:p.Glu8358Val
|
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XM_017010612.1:c.25022A>T
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XP_016866101.1:p.Glu8341Val
|
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XM_017010613.1:c.25028A>T
|
XP_016866102.1:p.Glu8343Val
|
|
XM_017010614.1:c.24944A>T
|
XP_016866103.1:p.Glu8315Val
|
|
XM_017010615.1:c.24875A>T
|
XP_016866104.1:p.Glu8292Val
|
|
XM_017010616.1:c.25031A>T
|
XP_016866105.1:p.Glu8344Val
|
|
XM_017010617.1:c.25028A>T
|
XP_016866106.1:p.Glu8343Val
|
|
XM_017010618.1:c.25016A>T
|
XP_016866107.1:p.Glu8339Val
|
|
XM_017010619.1:c.23375A>T
|
XP_016866108.1:p.Glu7792Val
|
|
NM_182961.4:c.24995A>T
MANE Select
|
NP_892006.3:p.Glu8332Val
|
|
NM_001347701.2:c.1601A>T
|
NP_001334630.1:p.Glu534Val
|
|
NM_001347702.2:c.1529A>T
MANE Plus Clinical
|
NP_001334631.1:p.Glu510Val
|
|
NM_033071.5:c.24851A>T
|
NP_149062.2:p.Glu8284Val
|
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