ENST00000354674.5:c.592G>T
MANE Plus Clinical
|
ENSP00000346701.4:p.Glu198Ter
|
|
ENST00000367255.10:c.24127G>T
MANE Select
|
ENSP00000356224.5:p.Glu8043Ter
|
|
ENST00000423061.6:c.23914G>T
|
ENSP00000396024.1:p.Glu7972Ter
|
|
ENST00000673173.1:c.41G>T
|
|
|
ENST00000341594.9:c.22912G>T
|
ENSP00000341887.6:p.Glu7638Ter
|
|
ENST00000347037.9:n.806G>T
|
|
|
ENST00000354674.4:c.592G>T
|
ENSP00000346701.4:p.Glu198Ter
|
|
ENST00000367251.7:c.2893G>T
|
ENSP00000356220.3:p.Glu965Ter
|
|
ENST00000367255.9:c.24127G>T
|
ENSP00000356224.5:p.Glu8043Ter
|
|
ENST00000367256.9:n.7819G>T
|
|
|
ENST00000367257.8:c.2065G>T
|
ENSP00000356226.4:p.Glu689Ter
|
|
ENST00000409694.6:n.7711G>T
|
|
|
ENST00000423061.5:c.23914G>T
|
ENSP00000396024.1:p.Glu7972Ter
|
|
ENST00000460912.6:n.672G>T
|
|
|
ENST00000476519.1:n.189G>T
|
|
|
ENST00000490866.2:n.502G>T
|
|
|
ENST00000536990.5:n.964G>T
|
|
|
ENST00000539504.5:c.592G>T
|
ENSP00000441052.1:p.Glu198Ter
|
|
NM_033071.3:c.23914G>T
|
NP_149062.1:p.Glu7972Ter
|
|
NM_182961.3:c.24127G>T
|
NP_892006.3:p.Glu8043Ter
|
|
XM_006715407.1:c.24163G>T
|
XP_006715470.1:p.Glu8055Ter
|
|
XM_006715408.1:c.24151G>T
|
XP_006715471.1:p.Glu8051Ter
|
|
XM_006715409.1:c.24142G>T
|
XP_006715472.1:p.Glu8048Ter
|
|
XM_006715410.1:c.24163G>T
|
XP_006715473.1:p.Glu8055Ter
|
|
XM_006715411.1:c.24112G>T
|
XP_006715474.1:p.Glu8038Ter
|
|
XM_006715412.1:c.24148G>T
|
XP_006715475.1:p.Glu8050Ter
|
|
XM_006715413.1:c.24163G>T
|
XP_006715476.1:p.Glu8055Ter
|
|
XM_006715414.1:c.24091G>T
|
XP_006715477.1:p.Glu8031Ter
|
|
XM_006715415.1:c.24163G>T
|
XP_006715478.1:p.Glu8055Ter
|
|
XM_006715416.1:c.24148G>T
|
XP_006715479.1:p.Glu8050Ter
|
|
XM_006715417.1:c.24022G>T
|
XP_006715480.1:p.Glu8008Ter
|
|
XM_006715420.1:c.24010G>T
|
XP_006715483.1:p.Glu8004Ter
|
|
XM_006715421.1:c.24007G>T
|
XP_006715484.1:p.Glu8003Ter
|
|
XM_006715422.1:c.24004G>T
|
XP_006715485.1:p.Glu8002Ter
|
|
XM_006715423.1:c.24163G>T
|
XP_006715486.1:p.Glu8055Ter
|
|
XM_006715424.1:c.24163G>T
|
XP_006715487.1:p.Glu8055Ter
|
|
XM_006715425.1:c.24163G>T
|
XP_006715488.1:p.Glu8055Ter
|
|
XM_011535641.1:c.24160G>T
|
XP_011533943.1:p.Glu8054Ter
|
|
XM_011535642.1:c.24148G>T
|
XP_011533944.1:p.Glu8050Ter
|
|
XM_011535643.1:c.23998G>T
|
XP_011533945.1:p.Glu8000Ter
|
|
XM_011535644.1:c.22438G>T
|
XP_011533946.1:p.Glu7480Ter
|
|
XM_011535645.1:c.21931G>T
|
XP_011533947.1:p.Glu7311Ter
|
|
XM_011535647.1:c.17398G>T
|
XP_011533949.1:p.Glu5800Ter
|
|
NM_001347701.1:c.733G>T
|
NP_001334630.1:p.Glu245Ter
|
|
NM_001347702.1:c.592G>T
|
NP_001334631.1:p.Glu198Ter
|
|
XM_006715408.2:c.24151G>T
|
XP_006715471.1:p.Glu8051Ter
|
|
XM_006715410.2:c.24163G>T
|
XP_006715473.1:p.Glu8055Ter
|
|
XM_006715412.2:c.24148G>T
|
XP_006715475.1:p.Glu8050Ter
|
|
XM_006715413.2:c.24163G>T
|
XP_006715476.1:p.Glu8055Ter
|
|
XM_006715415.2:c.24163G>T
|
XP_006715478.1:p.Glu8055Ter
|
|
XM_006715416.2:c.24148G>T
|
XP_006715479.1:p.Glu8050Ter
|
|
XM_006715417.2:c.24022G>T
|
XP_006715480.1:p.Glu8008Ter
|
|
XM_006715420.2:c.24010G>T
|
XP_006715483.1:p.Glu8004Ter
|
|
XM_006715421.2:c.24007G>T
|
XP_006715484.1:p.Glu8003Ter
|
|
XM_006715423.2:c.24163G>T
|
XP_006715486.1:p.Glu8055Ter
|
|
XM_006715424.2:c.24163G>T
|
XP_006715487.1:p.Glu8055Ter
|
|
XM_006715425.2:c.24163G>T
|
XP_006715488.1:p.Glu8055Ter
|
|
XM_011535641.2:c.24160G>T
|
XP_011533943.1:p.Glu8054Ter
|
|
XM_011535642.2:c.24148G>T
|
XP_011533944.1:p.Glu8050Ter
|
|
XM_011535645.2:c.21931G>T
|
XP_011533947.1:p.Glu7311Ter
|
|
XM_017010608.1:c.24163G>T
|
XP_016866097.1:p.Glu8055Ter
|
|
XM_017010609.1:c.24163G>T
|
XP_016866098.1:p.Glu8055Ter
|
|
XM_017010610.1:c.24142G>T
|
XP_016866099.1:p.Glu8048Ter
|
|
XM_017010611.2:c.24136G>T
|
XP_016866100.1:p.Glu8046Ter
|
|
XM_017010612.1:c.24085G>T
|
XP_016866101.1:p.Glu8029Ter
|
|
XM_017010613.1:c.24160G>T
|
XP_016866102.1:p.Glu8054Ter
|
|
XM_017010614.1:c.24007G>T
|
XP_016866103.1:p.Glu8003Ter
|
|
XM_017010615.1:c.24007G>T
|
XP_016866104.1:p.Glu8003Ter
|
|
XM_017010616.1:c.24163G>T
|
XP_016866105.1:p.Glu8055Ter
|
|
XM_017010617.1:c.24160G>T
|
XP_016866106.1:p.Glu8054Ter
|
|
XM_017010618.1:c.24148G>T
|
XP_016866107.1:p.Glu8050Ter
|
|
XM_017010619.1:c.22438G>T
|
XP_016866108.1:p.Glu7480Ter
|
|
NM_182961.4:c.24127G>T
MANE Select
|
NP_892006.3:p.Glu8043Ter
|
|
NM_001347701.2:c.733G>T
|
NP_001334630.1:p.Glu245Ter
|
|
NM_001347702.2:c.592G>T
MANE Plus Clinical
|
NP_001334631.1:p.Glu198Ter
|
|
NM_033071.5:c.23914G>T
|
NP_149062.2:p.Glu7972Ter
|
|