ENST00000354674.5:c.2829A>C
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Val943=
|
|
ENST00000367255.10:c.26295A>C
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Val8765=
|
|
ENST00000423061.6:c.26151A>C
(SYNE1)
|
ENSP00000396024.1:p.Val8717=
|
|
ENST00000672154.1:c.1638A>C
(SYNE1)
|
|
|
ENST00000672169.1:c.2013A>C
(SYNE1)
|
|
|
ENST00000673173.1:c.1880A>C
(SYNE1)
|
|
|
ENST00000673451.1:c.2145A>C
(SYNE1)
|
ENSP00000500189.1:n.2145A>C
|
|
ENST00000341594.9:c.25080A>C
(SYNE1)
|
ENSP00000341887.6:p.Val8360=
|
|
ENST00000347037.9:n.3043A>C
(SYNE1)
|
|
|
ENST00000354674.4:c.2829A>C
(SYNE1)
|
ENSP00000346701.4:p.Val943=
|
|
ENST00000367251.7:c.5071A>C
(SYNE1)
|
ENSP00000356220.3:n.5071A>C
|
|
ENST00000367255.9:c.26295A>C
(SYNE1)
|
ENSP00000356224.5:p.Val8765=
|
|
ENST00000367256.9:n.9987A>C
(SYNE1)
|
|
|
ENST00000367257.8:c.4174A>C
(SYNE1)
|
ENSP00000356226.4:n.4174A>C
|
|
ENST00000409694.6:n.9879A>C
(SYNE1)
|
|
|
ENST00000423061.5:c.26151A>C
(SYNE1)
|
ENSP00000396024.1:p.Val8717=
|
|
ENST00000427531.6:c.851-2731T>G
(ESR1)
|
ENSP00000394721.2:n.851-2731T>G
|
|
ENST00000460912.6:n.2909A>C
(SYNE1)
|
|
|
ENST00000478916.5:n.6932A>C
(SYNE1)
|
|
|
ENST00000539504.5:c.2760A>C
(SYNE1)
|
ENSP00000441052.1:p.Val920=
|
|
NM_033071.3:c.26151A>C
(SYNE1)
|
NP_149062.1:p.Val8717=
|
|
NM_182961.3:c.26295A>C
(SYNE1)
|
NP_892006.3:p.Val8765=
|
|
XM_006715407.1:c.26442A>C
(SYNE1)
|
XP_006715470.1:p.Val8814=
|
|
XM_006715408.1:c.26430A>C
(SYNE1)
|
XP_006715471.1:p.Val8810=
|
|
XM_006715409.1:c.26421A>C
(SYNE1)
|
XP_006715472.1:p.Val8807=
|
|
XM_006715410.1:c.26400A>C
(SYNE1)
|
XP_006715473.1:p.Val8800=
|
|
XM_006715411.1:c.26391A>C
(SYNE1)
|
XP_006715474.1:p.Val8797=
|
|
XM_006715412.1:c.26385A>C
(SYNE1)
|
XP_006715475.1:p.Val8795=
|
|
XM_006715413.1:c.26373A>C
(SYNE1)
|
XP_006715476.1:p.Val8791=
|
|
XM_006715414.1:c.26370A>C
(SYNE1)
|
XP_006715477.1:p.Val8790=
|
|
XM_006715415.1:c.26331A>C
(SYNE1)
|
XP_006715478.1:p.Val8777=
|
|
XM_006715416.1:c.26316A>C
(SYNE1)
|
XP_006715479.1:p.Val8772=
|
|
XM_006715417.1:c.26301A>C
(SYNE1)
|
XP_006715480.1:p.Val8767=
|
|
XM_006715420.1:c.26289A>C
(SYNE1)
|
XP_006715483.1:p.Val8763=
|
|
XM_006715421.1:c.26286A>C
(SYNE1)
|
XP_006715484.1:p.Val8762=
|
|
XM_006715422.1:c.26283A>C
(SYNE1)
|
XP_006715485.1:p.Val8761=
|
|
XM_006715423.1:c.*106A>C
(SYNE1)
|
XP_006715486.1:n.*106A>C
|
|
XM_006715424.1:c.*106A>C
(SYNE1)
|
XP_006715487.1:n.*106A>C
|
|
XM_006715425.1:c.*106A>C
(SYNE1)
|
XP_006715488.1:n.*106A>C
|
|
XM_011535641.1:c.26439A>C
(SYNE1)
|
XP_011533943.1:p.Val8813=
|
|
XM_011535642.1:c.26427A>C
(SYNE1)
|
XP_011533944.1:p.Val8809=
|
|
XM_011535643.1:c.26277A>C
(SYNE1)
|
XP_011533945.1:p.Val8759=
|
|
XM_011535644.1:c.24717A>C
(SYNE1)
|
XP_011533946.1:p.Val8239=
|
|
XM_011535645.1:c.24210A>C
(SYNE1)
|
XP_011533947.1:p.Val8070=
|
|
XM_011535647.1:c.19677A>C
(SYNE1)
|
XP_011533949.1:p.Val6559=
|
|
NM_001328100.1:c.851-2731T>G
(ESR1)
|
NP_001315029.1:n.851-2731T>G
|
|
NM_001347701.1:c.*106A>C
(SYNE1)
|
NP_001334630.1:n.*106A>C
|
|
NM_001347702.1:c.2829A>C
(SYNE1)
|
NP_001334631.1:p.Val943=
|
|
XM_006715408.2:c.26430A>C
(SYNE1)
|
XP_006715471.1:p.Val8810=
|
|
XM_006715410.2:c.26400A>C
(SYNE1)
|
XP_006715473.1:p.Val8800=
|
|
XM_006715412.2:c.26385A>C
(SYNE1)
|
XP_006715475.1:p.Val8795=
|
|
XM_006715413.2:c.26373A>C
(SYNE1)
|
XP_006715476.1:p.Val8791=
|
|
XM_006715415.2:c.26331A>C
(SYNE1)
|
XP_006715478.1:p.Val8777=
|
|
XM_006715416.2:c.26316A>C
(SYNE1)
|
XP_006715479.1:p.Val8772=
|
|
XM_006715417.2:c.26301A>C
(SYNE1)
|
XP_006715480.1:p.Val8767=
|
|
XM_006715420.2:c.26289A>C
(SYNE1)
|
XP_006715483.1:p.Val8763=
|
|
XM_006715421.2:c.26286A>C
(SYNE1)
|
XP_006715484.1:p.Val8762=
|
|
XM_006715423.2:c.*106A>C
(SYNE1)
|
XP_006715486.1:n.*106A>C
|
|
XM_006715424.2:c.*106A>C
(SYNE1)
|
XP_006715487.1:n.*106A>C
|
|
XM_006715425.2:c.*106A>C
(SYNE1)
|
XP_006715488.1:n.*106A>C
|
|
XM_011535641.2:c.26439A>C
(SYNE1)
|
XP_011533943.1:p.Val8813=
|
|
XM_011535642.2:c.26427A>C
(SYNE1)
|
XP_011533944.1:p.Val8809=
|
|
XM_011535645.2:c.24210A>C
(SYNE1)
|
XP_011533947.1:p.Val8070=
|
|
XM_017010608.1:c.26442A>C
(SYNE1)
|
XP_016866097.1:p.Val8814=
|
|
XM_017010609.1:c.26442A>C
(SYNE1)
|
XP_016866098.1:p.Val8814=
|
|
XM_017010610.1:c.26421A>C
(SYNE1)
|
XP_016866099.1:p.Val8807=
|
|
XM_017010611.2:c.26415A>C
(SYNE1)
|
XP_016866100.1:p.Val8805=
|
|
XM_017010612.1:c.26364A>C
(SYNE1)
|
XP_016866101.1:p.Val8788=
|
|
XM_017010613.1:c.26328A>C
(SYNE1)
|
XP_016866102.1:p.Val8776=
|
|
XM_017010614.1:c.26286A>C
(SYNE1)
|
XP_016866103.1:p.Val8762=
|
|
XM_017010615.1:c.26175A>C
(SYNE1)
|
XP_016866104.1:p.Val8725=
|
|
XM_017010616.1:c.*106A>C
(SYNE1)
|
XP_016866105.1:n.*106A>C
|
|
XM_017010617.1:c.*106A>C
(SYNE1)
|
XP_016866106.1:n.*106A>C
|
|
XM_017010618.1:c.*106A>C
(SYNE1)
|
XP_016866107.1:n.*106A>C
|
|
XM_017010619.1:c.24717A>C
(SYNE1)
|
XP_016866108.1:p.Val8239=
|
|
NM_182961.4:c.26295A>C
(SYNE1)
MANE Select
|
NP_892006.3:p.Val8765=
|
|
NM_001328100.2:c.851-2731T>G
(ESR1)
|
NP_001315029.1:n.851-2731T>G
|
|
NM_001347701.2:c.*106A>C
(SYNE1)
|
NP_001334630.1:n.*106A>C
|
|
NM_001347702.2:c.2829A>C
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Val943=
|
|
NM_033071.5:c.26151A>C
(SYNE1)
|
NP_149062.2:p.Val8717=
|
|