|
ENST00000354674.5:c.2745C>A
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Gly915=
|
|
|
ENST00000367255.10:c.26211C>A
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Gly8737=
|
|
|
ENST00000423061.6:c.26067C>A
(SYNE1)
|
ENSP00000396024.1:p.Gly8689=
|
|
|
ENST00000672154.1:c.1554C>A
(SYNE1)
|
|
|
|
ENST00000672169.1:c.1929C>A
(SYNE1)
|
|
|
|
ENST00000673173.1:c.1796C>A
(SYNE1)
|
|
|
|
ENST00000673451.1:c.2061C>A
(SYNE1)
|
ENSP00000500189.1:n.2061C>A
|
|
|
ENST00000341594.9:c.24996C>A
(SYNE1)
|
ENSP00000341887.6:p.Gly8332=
|
|
|
ENST00000347037.9:n.2959C>A
(SYNE1)
|
|
|
|
ENST00000354674.4:c.2745C>A
(SYNE1)
|
ENSP00000346701.4:p.Gly915=
|
|
|
ENST00000367251.7:c.4987C>A
(SYNE1)
|
ENSP00000356220.3:n.4987C>A
|
|
|
ENST00000367255.9:c.26211C>A
(SYNE1)
|
ENSP00000356224.5:p.Gly8737=
|
|
|
ENST00000367256.9:n.9903C>A
(SYNE1)
|
|
|
|
ENST00000367257.8:c.4090C>A
(SYNE1)
|
ENSP00000356226.4:n.4090C>A
|
|
|
ENST00000409694.6:n.9795C>A
(SYNE1)
|
|
|
|
ENST00000423061.5:c.26067C>A
(SYNE1)
|
ENSP00000396024.1:p.Gly8689=
|
|
|
ENST00000427531.6:c.851-2647G>T
(ESR1)
|
ENSP00000394721.2:n.851-2647G>T
|
|
|
ENST00000460912.6:n.2825C>A
(SYNE1)
|
|
|
|
ENST00000478916.5:n.6848C>A
(SYNE1)
|
|
|
|
ENST00000536990.5:n.2989C>A
(SYNE1)
|
|
|
|
ENST00000539504.5:c.2676C>A
(SYNE1)
|
ENSP00000441052.1:p.Gly892=
|
|
|
NM_033071.3:c.26067C>A
(SYNE1)
|
NP_149062.1:p.Gly8689=
|
|
|
NM_182961.3:c.26211C>A
(SYNE1)
|
NP_892006.3:p.Gly8737=
|
|
|
XM_006715407.1:c.26358C>A
(SYNE1)
|
XP_006715470.1:p.Gly8786=
|
|
|
XM_006715408.1:c.26346C>A
(SYNE1)
|
XP_006715471.1:p.Gly8782=
|
|
|
XM_006715409.1:c.26337C>A
(SYNE1)
|
XP_006715472.1:p.Gly8779=
|
|
|
XM_006715410.1:c.26316C>A
(SYNE1)
|
XP_006715473.1:p.Gly8772=
|
|
|
XM_006715411.1:c.26307C>A
(SYNE1)
|
XP_006715474.1:p.Gly8769=
|
|
|
XM_006715412.1:c.26301C>A
(SYNE1)
|
XP_006715475.1:p.Gly8767=
|
|
|
XM_006715413.1:c.26289C>A
(SYNE1)
|
XP_006715476.1:p.Gly8763=
|
|
|
XM_006715414.1:c.26286C>A
(SYNE1)
|
XP_006715477.1:p.Gly8762=
|
|
|
XM_006715415.1:c.26247C>A
(SYNE1)
|
XP_006715478.1:p.Gly8749=
|
|
|
XM_006715416.1:c.26232C>A
(SYNE1)
|
XP_006715479.1:p.Gly8744=
|
|
|
XM_006715417.1:c.26217C>A
(SYNE1)
|
XP_006715480.1:p.Gly8739=
|
|
|
XM_006715420.1:c.26205C>A
(SYNE1)
|
XP_006715483.1:p.Gly8735=
|
|
|
XM_006715421.1:c.26202C>A
(SYNE1)
|
XP_006715484.1:p.Gly8734=
|
|
|
XM_006715422.1:c.26199C>A
(SYNE1)
|
XP_006715485.1:p.Gly8733=
|
|
|
XM_006715423.1:c.*22C>A
(SYNE1)
|
XP_006715486.1:n.*22C>A
|
|
|
XM_006715424.1:c.*22C>A
(SYNE1)
|
XP_006715487.1:n.*22C>A
|
|
|
XM_006715425.1:c.*22C>A
(SYNE1)
|
XP_006715488.1:n.*22C>A
|
|
|
XM_011535641.1:c.26355C>A
(SYNE1)
|
XP_011533943.1:p.Gly8785=
|
|
|
XM_011535642.1:c.26343C>A
(SYNE1)
|
XP_011533944.1:p.Gly8781=
|
|
|
XM_011535643.1:c.26193C>A
(SYNE1)
|
XP_011533945.1:p.Gly8731=
|
|
|
XM_011535644.1:c.24633C>A
(SYNE1)
|
XP_011533946.1:p.Gly8211=
|
|
|
XM_011535645.1:c.24126C>A
(SYNE1)
|
XP_011533947.1:p.Gly8042=
|
|
|
XM_011535647.1:c.19593C>A
(SYNE1)
|
XP_011533949.1:p.Gly6531=
|
|
|
NM_001328100.1:c.851-2647G>T
(ESR1)
|
NP_001315029.1:n.851-2647G>T
|
|
|
NM_001347701.1:c.*22C>A
(SYNE1)
|
NP_001334630.1:n.*22C>A
|
|
|
NM_001347702.1:c.2745C>A
(SYNE1)
|
NP_001334631.1:p.Gly915=
|
|
|
XM_006715408.2:c.26346C>A
(SYNE1)
|
XP_006715471.1:p.Gly8782=
|
|
|
XM_006715410.2:c.26316C>A
(SYNE1)
|
XP_006715473.1:p.Gly8772=
|
|
|
XM_006715412.2:c.26301C>A
(SYNE1)
|
XP_006715475.1:p.Gly8767=
|
|
|
XM_006715413.2:c.26289C>A
(SYNE1)
|
XP_006715476.1:p.Gly8763=
|
|
|
XM_006715415.2:c.26247C>A
(SYNE1)
|
XP_006715478.1:p.Gly8749=
|
|
|
XM_006715416.2:c.26232C>A
(SYNE1)
|
XP_006715479.1:p.Gly8744=
|
|
|
XM_006715417.2:c.26217C>A
(SYNE1)
|
XP_006715480.1:p.Gly8739=
|
|
|
XM_006715420.2:c.26205C>A
(SYNE1)
|
XP_006715483.1:p.Gly8735=
|
|
|
XM_006715421.2:c.26202C>A
(SYNE1)
|
XP_006715484.1:p.Gly8734=
|
|
|
XM_006715423.2:c.*22C>A
(SYNE1)
|
XP_006715486.1:n.*22C>A
|
|
|
XM_006715424.2:c.*22C>A
(SYNE1)
|
XP_006715487.1:n.*22C>A
|
|
|
XM_006715425.2:c.*22C>A
(SYNE1)
|
XP_006715488.1:n.*22C>A
|
|
|
XM_011535641.2:c.26355C>A
(SYNE1)
|
XP_011533943.1:p.Gly8785=
|
|
|
XM_011535642.2:c.26343C>A
(SYNE1)
|
XP_011533944.1:p.Gly8781=
|
|
|
XM_011535645.2:c.24126C>A
(SYNE1)
|
XP_011533947.1:p.Gly8042=
|
|
|
XM_017010608.1:c.26358C>A
(SYNE1)
|
XP_016866097.1:p.Gly8786=
|
|
|
XM_017010609.1:c.26358C>A
(SYNE1)
|
XP_016866098.1:p.Gly8786=
|
|
|
XM_017010610.1:c.26337C>A
(SYNE1)
|
XP_016866099.1:p.Gly8779=
|
|
|
XM_017010611.2:c.26331C>A
(SYNE1)
|
XP_016866100.1:p.Gly8777=
|
|
|
XM_017010612.1:c.26280C>A
(SYNE1)
|
XP_016866101.1:p.Gly8760=
|
|
|
XM_017010613.1:c.26244C>A
(SYNE1)
|
XP_016866102.1:p.Gly8748=
|
|
|
XM_017010614.1:c.26202C>A
(SYNE1)
|
XP_016866103.1:p.Gly8734=
|
|
|
XM_017010615.1:c.26091C>A
(SYNE1)
|
XP_016866104.1:p.Gly8697=
|
|
|
XM_017010616.1:c.*22C>A
(SYNE1)
|
XP_016866105.1:n.*22C>A
|
|
|
XM_017010617.1:c.*22C>A
(SYNE1)
|
XP_016866106.1:n.*22C>A
|
|
|
XM_017010618.1:c.*22C>A
(SYNE1)
|
XP_016866107.1:n.*22C>A
|
|
|
XM_017010619.1:c.24633C>A
(SYNE1)
|
XP_016866108.1:p.Gly8211=
|
|
|
NM_182961.4:c.26211C>A
(SYNE1)
MANE Select
|
NP_892006.3:p.Gly8737=
|
|
|
NM_001328100.2:c.851-2647G>T
(ESR1)
|
NP_001315029.1:n.851-2647G>T
|
|
|
NM_001347701.2:c.*22C>A
(SYNE1)
|
NP_001334630.1:n.*22C>A
|
|
|
NM_001347702.2:c.2745C>A
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Gly915=
|
|
|
NM_033071.5:c.26067C>A
(SYNE1)
|
NP_149062.2:p.Gly8689=
|
|
