ENST00000354674.5:c.1800G>C
MANE Plus Clinical
|
ENSP00000346701.4:p.Glu600Asp
|
|
ENST00000367255.10:c.25266G>C
MANE Select
|
ENSP00000356224.5:p.Glu8422Asp
|
|
ENST00000423061.6:c.25122G>C
|
ENSP00000396024.1:p.Glu8374Asp
|
|
ENST00000672154.1:c.668G>C
|
|
|
ENST00000672169.1:c.1001G>C
|
|
|
ENST00000673173.1:c.910G>C
|
|
|
ENST00000673451.1:c.1038G>C
|
ENSP00000500189.1:p.Glu346Asp
|
|
ENST00000341594.9:c.24051G>C
|
ENSP00000341887.6:p.Glu8017Asp
|
|
ENST00000347037.9:n.2014G>C
|
|
|
ENST00000354674.4:c.1800G>C
|
ENSP00000346701.4:p.Glu600Asp
|
|
ENST00000367251.7:c.4101G>C
|
ENSP00000356220.3:p.Glu1367Asp
|
|
ENST00000367255.9:c.25266G>C
|
ENSP00000356224.5:p.Glu8422Asp
|
|
ENST00000367256.9:n.8958G>C
|
|
|
ENST00000367257.8:c.3204G>C
|
ENSP00000356226.4:p.Glu1068Asp
|
|
ENST00000409694.6:n.8850G>C
|
|
|
ENST00000423061.5:c.25122G>C
|
ENSP00000396024.1:p.Glu8374Asp
|
|
ENST00000460912.6:n.1880G>C
|
|
|
ENST00000478916.5:n.4288G>C
|
|
|
ENST00000536990.5:n.2103G>C
|
|
|
ENST00000539504.5:c.1731G>C
|
ENSP00000441052.1:p.Glu577Asp
|
|
NM_033071.3:c.25122G>C
|
NP_149062.1:p.Glu8374Asp
|
|
NM_182961.3:c.25266G>C
|
NP_892006.3:p.Glu8422Asp
|
|
XM_006715407.1:c.25371G>C
|
XP_006715470.1:p.Glu8457Asp
|
|
XM_006715408.1:c.25359G>C
|
XP_006715471.1:p.Glu8453Asp
|
|
XM_006715409.1:c.25350G>C
|
XP_006715472.1:p.Glu8450Asp
|
|
XM_006715410.1:c.25371G>C
|
XP_006715473.1:p.Glu8457Asp
|
|
XM_006715411.1:c.25320G>C
|
XP_006715474.1:p.Glu8440Asp
|
|
XM_006715412.1:c.25356G>C
|
XP_006715475.1:p.Glu8452Asp
|
|
XM_006715413.1:c.25302G>C
|
XP_006715476.1:p.Glu8434Asp
|
|
XM_006715414.1:c.25299G>C
|
XP_006715477.1:p.Glu8433Asp
|
|
XM_006715415.1:c.25302G>C
|
XP_006715478.1:p.Glu8434Asp
|
|
XM_006715416.1:c.25287G>C
|
XP_006715479.1:p.Glu8429Asp
|
|
XM_006715417.1:c.25230G>C
|
XP_006715480.1:p.Glu8410Asp
|
|
XM_006715420.1:c.25218G>C
|
XP_006715483.1:p.Glu8406Asp
|
|
XM_006715421.1:c.25215G>C
|
XP_006715484.1:p.Glu8405Asp
|
|
XM_006715422.1:c.25212G>C
|
XP_006715485.1:p.Glu8404Asp
|
|
XM_006715423.1:c.25371G>C
|
XP_006715486.1:p.Glu8457Asp
|
|
XM_006715424.1:c.25371G>C
|
XP_006715487.1:p.Glu8457Asp
|
|
XM_006715425.1:c.25302G>C
|
XP_006715488.1:p.Glu8434Asp
|
|
XM_011535641.1:c.25368G>C
|
XP_011533943.1:p.Glu8456Asp
|
|
XM_011535642.1:c.25356G>C
|
XP_011533944.1:p.Glu8452Asp
|
|
XM_011535643.1:c.25206G>C
|
XP_011533945.1:p.Glu8402Asp
|
|
XM_011535644.1:c.23646G>C
|
XP_011533946.1:p.Glu7882Asp
|
|
XM_011535645.1:c.23139G>C
|
XP_011533947.1:p.Glu7713Asp
|
|
XM_011535647.1:c.18606G>C
|
XP_011533949.1:p.Glu6202Asp
|
|
NM_001347701.1:c.1872G>C
|
NP_001334630.1:p.Glu624Asp
|
|
NM_001347702.1:c.1800G>C
|
NP_001334631.1:p.Glu600Asp
|
|
XM_006715408.2:c.25359G>C
|
XP_006715471.1:p.Glu8453Asp
|
|
XM_006715410.2:c.25371G>C
|
XP_006715473.1:p.Glu8457Asp
|
|
XM_006715412.2:c.25356G>C
|
XP_006715475.1:p.Glu8452Asp
|
|
XM_006715413.2:c.25302G>C
|
XP_006715476.1:p.Glu8434Asp
|
|
XM_006715415.2:c.25302G>C
|
XP_006715478.1:p.Glu8434Asp
|
|
XM_006715416.2:c.25287G>C
|
XP_006715479.1:p.Glu8429Asp
|
|
XM_006715417.2:c.25230G>C
|
XP_006715480.1:p.Glu8410Asp
|
|
XM_006715420.2:c.25218G>C
|
XP_006715483.1:p.Glu8406Asp
|
|
XM_006715421.2:c.25215G>C
|
XP_006715484.1:p.Glu8405Asp
|
|
XM_006715423.2:c.25371G>C
|
XP_006715486.1:p.Glu8457Asp
|
|
XM_006715424.2:c.25371G>C
|
XP_006715487.1:p.Glu8457Asp
|
|
XM_006715425.2:c.25302G>C
|
XP_006715488.1:p.Glu8434Asp
|
|
XM_011535641.2:c.25368G>C
|
XP_011533943.1:p.Glu8456Asp
|
|
XM_011535642.2:c.25356G>C
|
XP_011533944.1:p.Glu8452Asp
|
|
XM_011535645.2:c.23139G>C
|
XP_011533947.1:p.Glu7713Asp
|
|
XM_017010608.1:c.25371G>C
|
XP_016866097.1:p.Glu8457Asp
|
|
XM_017010609.1:c.25371G>C
|
XP_016866098.1:p.Glu8457Asp
|
|
XM_017010610.1:c.25350G>C
|
XP_016866099.1:p.Glu8450Asp
|
|
XM_017010611.2:c.25344G>C
|
XP_016866100.1:p.Glu8448Asp
|
|
XM_017010612.1:c.25293G>C
|
XP_016866101.1:p.Glu8431Asp
|
|
XM_017010613.1:c.25299G>C
|
XP_016866102.1:p.Glu8433Asp
|
|
XM_017010614.1:c.25215G>C
|
XP_016866103.1:p.Glu8405Asp
|
|
XM_017010615.1:c.25146G>C
|
XP_016866104.1:p.Glu8382Asp
|
|
XM_017010616.1:c.25302G>C
|
XP_016866105.1:p.Glu8434Asp
|
|
XM_017010617.1:c.25299G>C
|
XP_016866106.1:p.Glu8433Asp
|
|
XM_017010618.1:c.25287G>C
|
XP_016866107.1:p.Glu8429Asp
|
|
XM_017010619.1:c.23646G>C
|
XP_016866108.1:p.Glu7882Asp
|
|
NM_182961.4:c.25266G>C
MANE Select
|
NP_892006.3:p.Glu8422Asp
|
|
NM_001347701.2:c.1872G>C
|
NP_001334630.1:p.Glu624Asp
|
|
NM_001347702.2:c.1800G>C
MANE Plus Clinical
|
NP_001334631.1:p.Glu600Asp
|
|
NM_033071.5:c.25122G>C
|
NP_149062.2:p.Glu8374Asp
|
|