ENST00000354674.5:c.1792C>A
MANE Plus Clinical
|
ENSP00000346701.4:p.Arg598=
|
|
ENST00000367255.10:c.25258C>A
MANE Select
|
ENSP00000356224.5:p.Arg8420=
|
|
ENST00000423061.6:c.25114C>A
|
ENSP00000396024.1:p.Arg8372=
|
|
ENST00000672154.1:c.660C>A
|
|
|
ENST00000672169.1:c.993C>A
|
|
|
ENST00000673173.1:c.902C>A
|
|
|
ENST00000673451.1:c.1030C>A
|
ENSP00000500189.1:p.Arg344=
|
|
ENST00000341594.9:c.24043C>A
|
ENSP00000341887.6:p.Arg8015=
|
|
ENST00000347037.9:n.2006C>A
|
|
|
ENST00000354674.4:c.1792C>A
|
ENSP00000346701.4:p.Arg598=
|
|
ENST00000367251.7:c.4093C>A
|
ENSP00000356220.3:p.Arg1365=
|
|
ENST00000367255.9:c.25258C>A
|
ENSP00000356224.5:p.Arg8420=
|
|
ENST00000367256.9:n.8950C>A
|
|
|
ENST00000367257.8:c.3196C>A
|
ENSP00000356226.4:p.Arg1066=
|
|
ENST00000409694.6:n.8842C>A
|
|
|
ENST00000423061.5:c.25114C>A
|
ENSP00000396024.1:p.Arg8372=
|
|
ENST00000460912.6:n.1872C>A
|
|
|
ENST00000478916.5:n.4280C>A
|
|
|
ENST00000536990.5:n.2095C>A
|
|
|
ENST00000539504.5:c.1723C>A
|
ENSP00000441052.1:p.Arg575=
|
|
NM_033071.3:c.25114C>A
|
NP_149062.1:p.Arg8372=
|
|
NM_182961.3:c.25258C>A
|
NP_892006.3:p.Arg8420=
|
|
XM_006715407.1:c.25363C>A
|
XP_006715470.1:p.Arg8455=
|
|
XM_006715408.1:c.25351C>A
|
XP_006715471.1:p.Arg8451=
|
|
XM_006715409.1:c.25342C>A
|
XP_006715472.1:p.Arg8448=
|
|
XM_006715410.1:c.25363C>A
|
XP_006715473.1:p.Arg8455=
|
|
XM_006715411.1:c.25312C>A
|
XP_006715474.1:p.Arg8438=
|
|
XM_006715412.1:c.25348C>A
|
XP_006715475.1:p.Arg8450=
|
|
XM_006715413.1:c.25294C>A
|
XP_006715476.1:p.Arg8432=
|
|
XM_006715414.1:c.25291C>A
|
XP_006715477.1:p.Arg8431=
|
|
XM_006715415.1:c.25294C>A
|
XP_006715478.1:p.Arg8432=
|
|
XM_006715416.1:c.25279C>A
|
XP_006715479.1:p.Arg8427=
|
|
XM_006715417.1:c.25222C>A
|
XP_006715480.1:p.Arg8408=
|
|
XM_006715420.1:c.25210C>A
|
XP_006715483.1:p.Arg8404=
|
|
XM_006715421.1:c.25207C>A
|
XP_006715484.1:p.Arg8403=
|
|
XM_006715422.1:c.25204C>A
|
XP_006715485.1:p.Arg8402=
|
|
XM_006715423.1:c.25363C>A
|
XP_006715486.1:p.Arg8455=
|
|
XM_006715424.1:c.25363C>A
|
XP_006715487.1:p.Arg8455=
|
|
XM_006715425.1:c.25294C>A
|
XP_006715488.1:p.Arg8432=
|
|
XM_011535641.1:c.25360C>A
|
XP_011533943.1:p.Arg8454=
|
|
XM_011535642.1:c.25348C>A
|
XP_011533944.1:p.Arg8450=
|
|
XM_011535643.1:c.25198C>A
|
XP_011533945.1:p.Arg8400=
|
|
XM_011535644.1:c.23638C>A
|
XP_011533946.1:p.Arg7880=
|
|
XM_011535645.1:c.23131C>A
|
XP_011533947.1:p.Arg7711=
|
|
XM_011535647.1:c.18598C>A
|
XP_011533949.1:p.Arg6200=
|
|
NM_001347701.1:c.1864C>A
|
NP_001334630.1:p.Arg622=
|
|
NM_001347702.1:c.1792C>A
|
NP_001334631.1:p.Arg598=
|
|
XM_006715408.2:c.25351C>A
|
XP_006715471.1:p.Arg8451=
|
|
XM_006715410.2:c.25363C>A
|
XP_006715473.1:p.Arg8455=
|
|
XM_006715412.2:c.25348C>A
|
XP_006715475.1:p.Arg8450=
|
|
XM_006715413.2:c.25294C>A
|
XP_006715476.1:p.Arg8432=
|
|
XM_006715415.2:c.25294C>A
|
XP_006715478.1:p.Arg8432=
|
|
XM_006715416.2:c.25279C>A
|
XP_006715479.1:p.Arg8427=
|
|
XM_006715417.2:c.25222C>A
|
XP_006715480.1:p.Arg8408=
|
|
XM_006715420.2:c.25210C>A
|
XP_006715483.1:p.Arg8404=
|
|
XM_006715421.2:c.25207C>A
|
XP_006715484.1:p.Arg8403=
|
|
XM_006715423.2:c.25363C>A
|
XP_006715486.1:p.Arg8455=
|
|
XM_006715424.2:c.25363C>A
|
XP_006715487.1:p.Arg8455=
|
|
XM_006715425.2:c.25294C>A
|
XP_006715488.1:p.Arg8432=
|
|
XM_011535641.2:c.25360C>A
|
XP_011533943.1:p.Arg8454=
|
|
XM_011535642.2:c.25348C>A
|
XP_011533944.1:p.Arg8450=
|
|
XM_011535645.2:c.23131C>A
|
XP_011533947.1:p.Arg7711=
|
|
XM_017010608.1:c.25363C>A
|
XP_016866097.1:p.Arg8455=
|
|
XM_017010609.1:c.25363C>A
|
XP_016866098.1:p.Arg8455=
|
|
XM_017010610.1:c.25342C>A
|
XP_016866099.1:p.Arg8448=
|
|
XM_017010611.2:c.25336C>A
|
XP_016866100.1:p.Arg8446=
|
|
XM_017010612.1:c.25285C>A
|
XP_016866101.1:p.Arg8429=
|
|
XM_017010613.1:c.25291C>A
|
XP_016866102.1:p.Arg8431=
|
|
XM_017010614.1:c.25207C>A
|
XP_016866103.1:p.Arg8403=
|
|
XM_017010615.1:c.25138C>A
|
XP_016866104.1:p.Arg8380=
|
|
XM_017010616.1:c.25294C>A
|
XP_016866105.1:p.Arg8432=
|
|
XM_017010617.1:c.25291C>A
|
XP_016866106.1:p.Arg8431=
|
|
XM_017010618.1:c.25279C>A
|
XP_016866107.1:p.Arg8427=
|
|
XM_017010619.1:c.23638C>A
|
XP_016866108.1:p.Arg7880=
|
|
NM_182961.4:c.25258C>A
MANE Select
|
NP_892006.3:p.Arg8420=
|
|
NM_001347701.2:c.1864C>A
|
NP_001334630.1:p.Arg622=
|
|
NM_001347702.2:c.1792C>A
MANE Plus Clinical
|
NP_001334631.1:p.Arg598=
|
|
NM_033071.5:c.25114C>A
|
NP_149062.2:p.Arg8372=
|
|