ENST00000354674.5:c.2787T>A
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Leu929=
|
|
ENST00000367255.10:c.26253T>A
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Leu8751=
|
|
ENST00000423061.6:c.26109T>A
(SYNE1)
|
ENSP00000396024.1:p.Leu8703=
|
|
ENST00000672154.1:c.1596T>A
(SYNE1)
|
|
|
ENST00000672169.1:c.1971T>A
(SYNE1)
|
|
|
ENST00000673173.1:c.1838T>A
(SYNE1)
|
|
|
ENST00000673451.1:c.2103T>A
(SYNE1)
|
ENSP00000500189.1:n.2103T>A
|
|
ENST00000341594.9:c.25038T>A
(SYNE1)
|
ENSP00000341887.6:p.Leu8346=
|
|
ENST00000347037.9:n.3001T>A
(SYNE1)
|
|
|
ENST00000354674.4:c.2787T>A
(SYNE1)
|
ENSP00000346701.4:p.Leu929=
|
|
ENST00000367251.7:c.5029T>A
(SYNE1)
|
ENSP00000356220.3:n.5029T>A
|
|
ENST00000367255.9:c.26253T>A
(SYNE1)
|
ENSP00000356224.5:p.Leu8751=
|
|
ENST00000367256.9:n.9945T>A
(SYNE1)
|
|
|
ENST00000367257.8:c.4132T>A
(SYNE1)
|
ENSP00000356226.4:n.4132T>A
|
|
ENST00000409694.6:n.9837T>A
(SYNE1)
|
|
|
ENST00000423061.5:c.26109T>A
(SYNE1)
|
ENSP00000396024.1:p.Leu8703=
|
|
ENST00000427531.6:c.851-2689A>T
(ESR1)
|
ENSP00000394721.2:n.851-2689A>T
|
|
ENST00000460912.6:n.2867T>A
(SYNE1)
|
|
|
ENST00000478916.5:n.6890T>A
(SYNE1)
|
|
|
ENST00000539504.5:c.2718T>A
(SYNE1)
|
ENSP00000441052.1:p.Leu906=
|
|
NM_033071.3:c.26109T>A
(SYNE1)
|
NP_149062.1:p.Leu8703=
|
|
NM_182961.3:c.26253T>A
(SYNE1)
|
NP_892006.3:p.Leu8751=
|
|
XM_006715407.1:c.26400T>A
(SYNE1)
|
XP_006715470.1:p.Leu8800=
|
|
XM_006715408.1:c.26388T>A
(SYNE1)
|
XP_006715471.1:p.Leu8796=
|
|
XM_006715409.1:c.26379T>A
(SYNE1)
|
XP_006715472.1:p.Leu8793=
|
|
XM_006715410.1:c.26358T>A
(SYNE1)
|
XP_006715473.1:p.Leu8786=
|
|
XM_006715411.1:c.26349T>A
(SYNE1)
|
XP_006715474.1:p.Leu8783=
|
|
XM_006715412.1:c.26343T>A
(SYNE1)
|
XP_006715475.1:p.Leu8781=
|
|
XM_006715413.1:c.26331T>A
(SYNE1)
|
XP_006715476.1:p.Leu8777=
|
|
XM_006715414.1:c.26328T>A
(SYNE1)
|
XP_006715477.1:p.Leu8776=
|
|
XM_006715415.1:c.26289T>A
(SYNE1)
|
XP_006715478.1:p.Leu8763=
|
|
XM_006715416.1:c.26274T>A
(SYNE1)
|
XP_006715479.1:p.Leu8758=
|
|
XM_006715417.1:c.26259T>A
(SYNE1)
|
XP_006715480.1:p.Leu8753=
|
|
XM_006715420.1:c.26247T>A
(SYNE1)
|
XP_006715483.1:p.Leu8749=
|
|
XM_006715421.1:c.26244T>A
(SYNE1)
|
XP_006715484.1:p.Leu8748=
|
|
XM_006715422.1:c.26241T>A
(SYNE1)
|
XP_006715485.1:p.Leu8747=
|
|
XM_006715423.1:c.*64T>A
(SYNE1)
|
XP_006715486.1:n.*64T>A
|
|
XM_006715424.1:c.*64T>A
(SYNE1)
|
XP_006715487.1:n.*64T>A
|
|
XM_006715425.1:c.*64T>A
(SYNE1)
|
XP_006715488.1:n.*64T>A
|
|
XM_011535641.1:c.26397T>A
(SYNE1)
|
XP_011533943.1:p.Leu8799=
|
|
XM_011535642.1:c.26385T>A
(SYNE1)
|
XP_011533944.1:p.Leu8795=
|
|
XM_011535643.1:c.26235T>A
(SYNE1)
|
XP_011533945.1:p.Leu8745=
|
|
XM_011535644.1:c.24675T>A
(SYNE1)
|
XP_011533946.1:p.Leu8225=
|
|
XM_011535645.1:c.24168T>A
(SYNE1)
|
XP_011533947.1:p.Leu8056=
|
|
XM_011535647.1:c.19635T>A
(SYNE1)
|
XP_011533949.1:p.Leu6545=
|
|
NM_001328100.1:c.851-2689A>T
(ESR1)
|
NP_001315029.1:n.851-2689A>T
|
|
NM_001347701.1:c.*64T>A
(SYNE1)
|
NP_001334630.1:n.*64T>A
|
|
NM_001347702.1:c.2787T>A
(SYNE1)
|
NP_001334631.1:p.Leu929=
|
|
XM_006715408.2:c.26388T>A
(SYNE1)
|
XP_006715471.1:p.Leu8796=
|
|
XM_006715410.2:c.26358T>A
(SYNE1)
|
XP_006715473.1:p.Leu8786=
|
|
XM_006715412.2:c.26343T>A
(SYNE1)
|
XP_006715475.1:p.Leu8781=
|
|
XM_006715413.2:c.26331T>A
(SYNE1)
|
XP_006715476.1:p.Leu8777=
|
|
XM_006715415.2:c.26289T>A
(SYNE1)
|
XP_006715478.1:p.Leu8763=
|
|
XM_006715416.2:c.26274T>A
(SYNE1)
|
XP_006715479.1:p.Leu8758=
|
|
XM_006715417.2:c.26259T>A
(SYNE1)
|
XP_006715480.1:p.Leu8753=
|
|
XM_006715420.2:c.26247T>A
(SYNE1)
|
XP_006715483.1:p.Leu8749=
|
|
XM_006715421.2:c.26244T>A
(SYNE1)
|
XP_006715484.1:p.Leu8748=
|
|
XM_006715423.2:c.*64T>A
(SYNE1)
|
XP_006715486.1:n.*64T>A
|
|
XM_006715424.2:c.*64T>A
(SYNE1)
|
XP_006715487.1:n.*64T>A
|
|
XM_006715425.2:c.*64T>A
(SYNE1)
|
XP_006715488.1:n.*64T>A
|
|
XM_011535641.2:c.26397T>A
(SYNE1)
|
XP_011533943.1:p.Leu8799=
|
|
XM_011535642.2:c.26385T>A
(SYNE1)
|
XP_011533944.1:p.Leu8795=
|
|
XM_011535645.2:c.24168T>A
(SYNE1)
|
XP_011533947.1:p.Leu8056=
|
|
XM_017010608.1:c.26400T>A
(SYNE1)
|
XP_016866097.1:p.Leu8800=
|
|
XM_017010609.1:c.26400T>A
(SYNE1)
|
XP_016866098.1:p.Leu8800=
|
|
XM_017010610.1:c.26379T>A
(SYNE1)
|
XP_016866099.1:p.Leu8793=
|
|
XM_017010611.2:c.26373T>A
(SYNE1)
|
XP_016866100.1:p.Leu8791=
|
|
XM_017010612.1:c.26322T>A
(SYNE1)
|
XP_016866101.1:p.Leu8774=
|
|
XM_017010613.1:c.26286T>A
(SYNE1)
|
XP_016866102.1:p.Leu8762=
|
|
XM_017010614.1:c.26244T>A
(SYNE1)
|
XP_016866103.1:p.Leu8748=
|
|
XM_017010615.1:c.26133T>A
(SYNE1)
|
XP_016866104.1:p.Leu8711=
|
|
XM_017010616.1:c.*64T>A
(SYNE1)
|
XP_016866105.1:n.*64T>A
|
|
XM_017010617.1:c.*64T>A
(SYNE1)
|
XP_016866106.1:n.*64T>A
|
|
XM_017010618.1:c.*64T>A
(SYNE1)
|
XP_016866107.1:n.*64T>A
|
|
XM_017010619.1:c.24675T>A
(SYNE1)
|
XP_016866108.1:p.Leu8225=
|
|
NM_182961.4:c.26253T>A
(SYNE1)
MANE Select
|
NP_892006.3:p.Leu8751=
|
|
NM_001328100.2:c.851-2689A>T
(ESR1)
|
NP_001315029.1:n.851-2689A>T
|
|
NM_001347701.2:c.*64T>A
(SYNE1)
|
NP_001334630.1:n.*64T>A
|
|
NM_001347702.2:c.2787T>A
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Leu929=
|
|
NM_033071.5:c.26109T>A
(SYNE1)
|
NP_149062.2:p.Leu8703=
|
|