ENST00000354674.5:c.2740T>G
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Ser914Ala
|
|
ENST00000367255.10:c.26206T>G
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Ser8736Ala
|
|
ENST00000423061.6:c.26062T>G
(SYNE1)
|
ENSP00000396024.1:p.Ser8688Ala
|
|
ENST00000672154.1:c.1549T>G
(SYNE1)
|
|
|
ENST00000672169.1:c.1924T>G
(SYNE1)
|
|
|
ENST00000673173.1:c.1791T>G
(SYNE1)
|
|
|
ENST00000673451.1:c.2056T>G
(SYNE1)
|
ENSP00000500189.1:n.2056T>G
|
|
ENST00000341594.9:c.24991T>G
(SYNE1)
|
ENSP00000341887.6:p.Ser8331Ala
|
|
ENST00000347037.9:n.2954T>G
(SYNE1)
|
|
|
ENST00000354674.4:c.2740T>G
(SYNE1)
|
ENSP00000346701.4:p.Ser914Ala
|
|
ENST00000367251.7:c.4982T>G
(SYNE1)
|
ENSP00000356220.3:n.4982T>G
|
|
ENST00000367255.9:c.26206T>G
(SYNE1)
|
ENSP00000356224.5:p.Ser8736Ala
|
|
ENST00000367256.9:n.9898T>G
(SYNE1)
|
|
|
ENST00000367257.8:c.4085T>G
(SYNE1)
|
ENSP00000356226.4:n.4085T>G
|
|
ENST00000409694.6:n.9790T>G
(SYNE1)
|
|
|
ENST00000423061.5:c.26062T>G
(SYNE1)
|
ENSP00000396024.1:p.Ser8688Ala
|
|
ENST00000427531.6:c.851-2642A>C
(ESR1)
|
ENSP00000394721.2:n.851-2642A>C
|
|
ENST00000460912.6:n.2820T>G
(SYNE1)
|
|
|
ENST00000478916.5:n.6843T>G
(SYNE1)
|
|
|
ENST00000536990.5:n.2984T>G
(SYNE1)
|
|
|
ENST00000539504.5:c.2671T>G
(SYNE1)
|
ENSP00000441052.1:p.Ser891Ala
|
|
NM_033071.3:c.26062T>G
(SYNE1)
|
NP_149062.1:p.Ser8688Ala
|
|
NM_182961.3:c.26206T>G
(SYNE1)
|
NP_892006.3:p.Ser8736Ala
|
|
XM_006715407.1:c.26353T>G
(SYNE1)
|
XP_006715470.1:p.Ser8785Ala
|
|
XM_006715408.1:c.26341T>G
(SYNE1)
|
XP_006715471.1:p.Ser8781Ala
|
|
XM_006715409.1:c.26332T>G
(SYNE1)
|
XP_006715472.1:p.Ser8778Ala
|
|
XM_006715410.1:c.26311T>G
(SYNE1)
|
XP_006715473.1:p.Ser8771Ala
|
|
XM_006715411.1:c.26302T>G
(SYNE1)
|
XP_006715474.1:p.Ser8768Ala
|
|
XM_006715412.1:c.26296T>G
(SYNE1)
|
XP_006715475.1:p.Ser8766Ala
|
|
XM_006715413.1:c.26284T>G
(SYNE1)
|
XP_006715476.1:p.Ser8762Ala
|
|
XM_006715414.1:c.26281T>G
(SYNE1)
|
XP_006715477.1:p.Ser8761Ala
|
|
XM_006715415.1:c.26242T>G
(SYNE1)
|
XP_006715478.1:p.Ser8748Ala
|
|
XM_006715416.1:c.26227T>G
(SYNE1)
|
XP_006715479.1:p.Ser8743Ala
|
|
XM_006715417.1:c.26212T>G
(SYNE1)
|
XP_006715480.1:p.Ser8738Ala
|
|
XM_006715420.1:c.26200T>G
(SYNE1)
|
XP_006715483.1:p.Ser8734Ala
|
|
XM_006715421.1:c.26197T>G
(SYNE1)
|
XP_006715484.1:p.Ser8733Ala
|
|
XM_006715422.1:c.26194T>G
(SYNE1)
|
XP_006715485.1:p.Ser8732Ala
|
|
XM_006715423.1:c.*17T>G
(SYNE1)
|
XP_006715486.1:n.*17T>G
|
|
XM_006715424.1:c.*17T>G
(SYNE1)
|
XP_006715487.1:n.*17T>G
|
|
XM_006715425.1:c.*17T>G
(SYNE1)
|
XP_006715488.1:n.*17T>G
|
|
XM_011535641.1:c.26350T>G
(SYNE1)
|
XP_011533943.1:p.Ser8784Ala
|
|
XM_011535642.1:c.26338T>G
(SYNE1)
|
XP_011533944.1:p.Ser8780Ala
|
|
XM_011535643.1:c.26188T>G
(SYNE1)
|
XP_011533945.1:p.Ser8730Ala
|
|
XM_011535644.1:c.24628T>G
(SYNE1)
|
XP_011533946.1:p.Ser8210Ala
|
|
XM_011535645.1:c.24121T>G
(SYNE1)
|
XP_011533947.1:p.Ser8041Ala
|
|
XM_011535647.1:c.19588T>G
(SYNE1)
|
XP_011533949.1:p.Ser6530Ala
|
|
NM_001328100.1:c.851-2642A>C
(ESR1)
|
NP_001315029.1:n.851-2642A>C
|
|
NM_001347701.1:c.*17T>G
(SYNE1)
|
NP_001334630.1:n.*17T>G
|
|
NM_001347702.1:c.2740T>G
(SYNE1)
|
NP_001334631.1:p.Ser914Ala
|
|
XM_006715408.2:c.26341T>G
(SYNE1)
|
XP_006715471.1:p.Ser8781Ala
|
|
XM_006715410.2:c.26311T>G
(SYNE1)
|
XP_006715473.1:p.Ser8771Ala
|
|
XM_006715412.2:c.26296T>G
(SYNE1)
|
XP_006715475.1:p.Ser8766Ala
|
|
XM_006715413.2:c.26284T>G
(SYNE1)
|
XP_006715476.1:p.Ser8762Ala
|
|
XM_006715415.2:c.26242T>G
(SYNE1)
|
XP_006715478.1:p.Ser8748Ala
|
|
XM_006715416.2:c.26227T>G
(SYNE1)
|
XP_006715479.1:p.Ser8743Ala
|
|
XM_006715417.2:c.26212T>G
(SYNE1)
|
XP_006715480.1:p.Ser8738Ala
|
|
XM_006715420.2:c.26200T>G
(SYNE1)
|
XP_006715483.1:p.Ser8734Ala
|
|
XM_006715421.2:c.26197T>G
(SYNE1)
|
XP_006715484.1:p.Ser8733Ala
|
|
XM_006715423.2:c.*17T>G
(SYNE1)
|
XP_006715486.1:n.*17T>G
|
|
XM_006715424.2:c.*17T>G
(SYNE1)
|
XP_006715487.1:n.*17T>G
|
|
XM_006715425.2:c.*17T>G
(SYNE1)
|
XP_006715488.1:n.*17T>G
|
|
XM_011535641.2:c.26350T>G
(SYNE1)
|
XP_011533943.1:p.Ser8784Ala
|
|
XM_011535642.2:c.26338T>G
(SYNE1)
|
XP_011533944.1:p.Ser8780Ala
|
|
XM_011535645.2:c.24121T>G
(SYNE1)
|
XP_011533947.1:p.Ser8041Ala
|
|
XM_017010608.1:c.26353T>G
(SYNE1)
|
XP_016866097.1:p.Ser8785Ala
|
|
XM_017010609.1:c.26353T>G
(SYNE1)
|
XP_016866098.1:p.Ser8785Ala
|
|
XM_017010610.1:c.26332T>G
(SYNE1)
|
XP_016866099.1:p.Ser8778Ala
|
|
XM_017010611.2:c.26326T>G
(SYNE1)
|
XP_016866100.1:p.Ser8776Ala
|
|
XM_017010612.1:c.26275T>G
(SYNE1)
|
XP_016866101.1:p.Ser8759Ala
|
|
XM_017010613.1:c.26239T>G
(SYNE1)
|
XP_016866102.1:p.Ser8747Ala
|
|
XM_017010614.1:c.26197T>G
(SYNE1)
|
XP_016866103.1:p.Ser8733Ala
|
|
XM_017010615.1:c.26086T>G
(SYNE1)
|
XP_016866104.1:p.Ser8696Ala
|
|
XM_017010616.1:c.*17T>G
(SYNE1)
|
XP_016866105.1:n.*17T>G
|
|
XM_017010617.1:c.*17T>G
(SYNE1)
|
XP_016866106.1:n.*17T>G
|
|
XM_017010618.1:c.*17T>G
(SYNE1)
|
XP_016866107.1:n.*17T>G
|
|
XM_017010619.1:c.24628T>G
(SYNE1)
|
XP_016866108.1:p.Ser8210Ala
|
|
NM_182961.4:c.26206T>G
(SYNE1)
MANE Select
|
NP_892006.3:p.Ser8736Ala
|
|
NM_001328100.2:c.851-2642A>C
(ESR1)
|
NP_001315029.1:n.851-2642A>C
|
|
NM_001347701.2:c.*17T>G
(SYNE1)
|
NP_001334630.1:n.*17T>G
|
|
NM_001347702.2:c.2740T>G
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Ser914Ala
|
|
NM_033071.5:c.26062T>G
(SYNE1)
|
NP_149062.2:p.Ser8688Ala
|
|