ENST00000354674.5:c.1749T>G
MANE Plus Clinical
|
ENSP00000346701.4:p.Val583=
|
|
ENST00000367255.10:c.25215T>G
MANE Select
|
ENSP00000356224.5:p.Val8405=
|
|
ENST00000423061.6:c.25071T>G
|
ENSP00000396024.1:p.Val8357=
|
|
ENST00000672154.1:c.617T>G
|
|
|
ENST00000672169.1:c.950T>G
|
|
|
ENST00000673173.1:c.891-1073T>G
|
|
|
ENST00000673451.1:c.987T>G
|
ENSP00000500189.1:p.Val329=
|
|
ENST00000341594.9:c.24000T>G
|
ENSP00000341887.6:p.Val8000=
|
|
ENST00000347037.9:n.1963T>G
|
|
|
ENST00000354674.4:c.1749T>G
|
ENSP00000346701.4:p.Val583=
|
|
ENST00000367251.7:c.4050T>G
|
ENSP00000356220.3:p.Val1350=
|
|
ENST00000367255.9:c.25215T>G
|
ENSP00000356224.5:p.Val8405=
|
|
ENST00000367256.9:n.8907T>G
|
|
|
ENST00000367257.8:c.3153T>G
|
ENSP00000356226.4:p.Val1051=
|
|
ENST00000409694.6:n.8799T>G
|
|
|
ENST00000423061.5:c.25071T>G
|
ENSP00000396024.1:p.Val8357=
|
|
ENST00000460912.6:n.1829T>G
|
|
|
ENST00000478916.5:n.4237T>G
|
|
|
ENST00000536990.5:n.2052T>G
|
|
|
ENST00000539504.5:c.1680T>G
|
ENSP00000441052.1:p.Val560=
|
|
NM_033071.3:c.25071T>G
|
NP_149062.1:p.Val8357=
|
|
NM_182961.3:c.25215T>G
|
NP_892006.3:p.Val8405=
|
|
XM_006715407.1:c.25320T>G
|
XP_006715470.1:p.Val8440=
|
|
XM_006715408.1:c.25308T>G
|
XP_006715471.1:p.Val8436=
|
|
XM_006715409.1:c.25299T>G
|
XP_006715472.1:p.Val8433=
|
|
XM_006715410.1:c.25320T>G
|
XP_006715473.1:p.Val8440=
|
|
XM_006715411.1:c.25269T>G
|
XP_006715474.1:p.Val8423=
|
|
XM_006715412.1:c.25305T>G
|
XP_006715475.1:p.Val8435=
|
|
XM_006715413.1:c.25251T>G
|
XP_006715476.1:p.Val8417=
|
|
XM_006715414.1:c.25248T>G
|
XP_006715477.1:p.Val8416=
|
|
XM_006715415.1:c.25251T>G
|
XP_006715478.1:p.Val8417=
|
|
XM_006715416.1:c.25236T>G
|
XP_006715479.1:p.Val8412=
|
|
XM_006715417.1:c.25179T>G
|
XP_006715480.1:p.Val8393=
|
|
XM_006715420.1:c.25167T>G
|
XP_006715483.1:p.Val8389=
|
|
XM_006715421.1:c.25164T>G
|
XP_006715484.1:p.Val8388=
|
|
XM_006715422.1:c.25161T>G
|
XP_006715485.1:p.Val8387=
|
|
XM_006715423.1:c.25320T>G
|
XP_006715486.1:p.Val8440=
|
|
XM_006715424.1:c.25320T>G
|
XP_006715487.1:p.Val8440=
|
|
XM_006715425.1:c.25251T>G
|
XP_006715488.1:p.Val8417=
|
|
XM_011535641.1:c.25317T>G
|
XP_011533943.1:p.Val8439=
|
|
XM_011535642.1:c.25305T>G
|
XP_011533944.1:p.Val8435=
|
|
XM_011535643.1:c.25155T>G
|
XP_011533945.1:p.Val8385=
|
|
XM_011535644.1:c.23595T>G
|
XP_011533946.1:p.Val7865=
|
|
XM_011535645.1:c.23088T>G
|
XP_011533947.1:p.Val7696=
|
|
XM_011535647.1:c.18555T>G
|
XP_011533949.1:p.Val6185=
|
|
NM_001347701.1:c.1821T>G
|
NP_001334630.1:p.Val607=
|
|
NM_001347702.1:c.1749T>G
|
NP_001334631.1:p.Val583=
|
|
XM_006715408.2:c.25308T>G
|
XP_006715471.1:p.Val8436=
|
|
XM_006715410.2:c.25320T>G
|
XP_006715473.1:p.Val8440=
|
|
XM_006715412.2:c.25305T>G
|
XP_006715475.1:p.Val8435=
|
|
XM_006715413.2:c.25251T>G
|
XP_006715476.1:p.Val8417=
|
|
XM_006715415.2:c.25251T>G
|
XP_006715478.1:p.Val8417=
|
|
XM_006715416.2:c.25236T>G
|
XP_006715479.1:p.Val8412=
|
|
XM_006715417.2:c.25179T>G
|
XP_006715480.1:p.Val8393=
|
|
XM_006715420.2:c.25167T>G
|
XP_006715483.1:p.Val8389=
|
|
XM_006715421.2:c.25164T>G
|
XP_006715484.1:p.Val8388=
|
|
XM_006715423.2:c.25320T>G
|
XP_006715486.1:p.Val8440=
|
|
XM_006715424.2:c.25320T>G
|
XP_006715487.1:p.Val8440=
|
|
XM_006715425.2:c.25251T>G
|
XP_006715488.1:p.Val8417=
|
|
XM_011535641.2:c.25317T>G
|
XP_011533943.1:p.Val8439=
|
|
XM_011535642.2:c.25305T>G
|
XP_011533944.1:p.Val8435=
|
|
XM_011535645.2:c.23088T>G
|
XP_011533947.1:p.Val7696=
|
|
XM_017010608.1:c.25320T>G
|
XP_016866097.1:p.Val8440=
|
|
XM_017010609.1:c.25320T>G
|
XP_016866098.1:p.Val8440=
|
|
XM_017010610.1:c.25299T>G
|
XP_016866099.1:p.Val8433=
|
|
XM_017010611.2:c.25293T>G
|
XP_016866100.1:p.Val8431=
|
|
XM_017010612.1:c.25242T>G
|
XP_016866101.1:p.Val8414=
|
|
XM_017010613.1:c.25248T>G
|
XP_016866102.1:p.Val8416=
|
|
XM_017010614.1:c.25164T>G
|
XP_016866103.1:p.Val8388=
|
|
XM_017010615.1:c.25095T>G
|
XP_016866104.1:p.Val8365=
|
|
XM_017010616.1:c.25251T>G
|
XP_016866105.1:p.Val8417=
|
|
XM_017010617.1:c.25248T>G
|
XP_016866106.1:p.Val8416=
|
|
XM_017010618.1:c.25236T>G
|
XP_016866107.1:p.Val8412=
|
|
XM_017010619.1:c.23595T>G
|
XP_016866108.1:p.Val7865=
|
|
NM_182961.4:c.25215T>G
MANE Select
|
NP_892006.3:p.Val8405=
|
|
NM_001347701.2:c.1821T>G
|
NP_001334630.1:p.Val607=
|
|
NM_001347702.2:c.1749T>G
MANE Plus Clinical
|
NP_001334631.1:p.Val583=
|
|
NM_033071.5:c.25071T>G
|
NP_149062.2:p.Val8357=
|
|