ENST00000354674.5:c.2778T>G
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Ala926=
|
|
ENST00000367255.10:c.26244T>G
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Ala8748=
|
|
ENST00000423061.6:c.26100T>G
(SYNE1)
|
ENSP00000396024.1:p.Ala8700=
|
|
ENST00000672154.1:c.1587T>G
(SYNE1)
|
|
|
ENST00000672169.1:c.1962T>G
(SYNE1)
|
|
|
ENST00000673173.1:c.1829T>G
(SYNE1)
|
|
|
ENST00000673451.1:c.2094T>G
(SYNE1)
|
ENSP00000500189.1:n.2094T>G
|
|
ENST00000341594.9:c.25029T>G
(SYNE1)
|
ENSP00000341887.6:p.Ala8343=
|
|
ENST00000347037.9:n.2992T>G
(SYNE1)
|
|
|
ENST00000354674.4:c.2778T>G
(SYNE1)
|
ENSP00000346701.4:p.Ala926=
|
|
ENST00000367251.7:c.5020T>G
(SYNE1)
|
ENSP00000356220.3:n.5020T>G
|
|
ENST00000367255.9:c.26244T>G
(SYNE1)
|
ENSP00000356224.5:p.Ala8748=
|
|
ENST00000367256.9:n.9936T>G
(SYNE1)
|
|
|
ENST00000367257.8:c.4123T>G
(SYNE1)
|
ENSP00000356226.4:n.4123T>G
|
|
ENST00000409694.6:n.9828T>G
(SYNE1)
|
|
|
ENST00000423061.5:c.26100T>G
(SYNE1)
|
ENSP00000396024.1:p.Ala8700=
|
|
ENST00000427531.6:c.851-2680A>C
(ESR1)
|
ENSP00000394721.2:n.851-2680A>C
|
|
ENST00000460912.6:n.2858T>G
(SYNE1)
|
|
|
ENST00000478916.5:n.6881T>G
(SYNE1)
|
|
|
ENST00000539504.5:c.2709T>G
(SYNE1)
|
ENSP00000441052.1:p.Ala903=
|
|
NM_033071.3:c.26100T>G
(SYNE1)
|
NP_149062.1:p.Ala8700=
|
|
NM_182961.3:c.26244T>G
(SYNE1)
|
NP_892006.3:p.Ala8748=
|
|
XM_006715407.1:c.26391T>G
(SYNE1)
|
XP_006715470.1:p.Ala8797=
|
|
XM_006715408.1:c.26379T>G
(SYNE1)
|
XP_006715471.1:p.Ala8793=
|
|
XM_006715409.1:c.26370T>G
(SYNE1)
|
XP_006715472.1:p.Ala8790=
|
|
XM_006715410.1:c.26349T>G
(SYNE1)
|
XP_006715473.1:p.Ala8783=
|
|
XM_006715411.1:c.26340T>G
(SYNE1)
|
XP_006715474.1:p.Ala8780=
|
|
XM_006715412.1:c.26334T>G
(SYNE1)
|
XP_006715475.1:p.Ala8778=
|
|
XM_006715413.1:c.26322T>G
(SYNE1)
|
XP_006715476.1:p.Ala8774=
|
|
XM_006715414.1:c.26319T>G
(SYNE1)
|
XP_006715477.1:p.Ala8773=
|
|
XM_006715415.1:c.26280T>G
(SYNE1)
|
XP_006715478.1:p.Ala8760=
|
|
XM_006715416.1:c.26265T>G
(SYNE1)
|
XP_006715479.1:p.Ala8755=
|
|
XM_006715417.1:c.26250T>G
(SYNE1)
|
XP_006715480.1:p.Ala8750=
|
|
XM_006715420.1:c.26238T>G
(SYNE1)
|
XP_006715483.1:p.Ala8746=
|
|
XM_006715421.1:c.26235T>G
(SYNE1)
|
XP_006715484.1:p.Ala8745=
|
|
XM_006715422.1:c.26232T>G
(SYNE1)
|
XP_006715485.1:p.Ala8744=
|
|
XM_006715423.1:c.*55T>G
(SYNE1)
|
XP_006715486.1:n.*55T>G
|
|
XM_006715424.1:c.*55T>G
(SYNE1)
|
XP_006715487.1:n.*55T>G
|
|
XM_006715425.1:c.*55T>G
(SYNE1)
|
XP_006715488.1:n.*55T>G
|
|
XM_011535641.1:c.26388T>G
(SYNE1)
|
XP_011533943.1:p.Ala8796=
|
|
XM_011535642.1:c.26376T>G
(SYNE1)
|
XP_011533944.1:p.Ala8792=
|
|
XM_011535643.1:c.26226T>G
(SYNE1)
|
XP_011533945.1:p.Ala8742=
|
|
XM_011535644.1:c.24666T>G
(SYNE1)
|
XP_011533946.1:p.Ala8222=
|
|
XM_011535645.1:c.24159T>G
(SYNE1)
|
XP_011533947.1:p.Ala8053=
|
|
XM_011535647.1:c.19626T>G
(SYNE1)
|
XP_011533949.1:p.Ala6542=
|
|
NM_001328100.1:c.851-2680A>C
(ESR1)
|
NP_001315029.1:n.851-2680A>C
|
|
NM_001347701.1:c.*55T>G
(SYNE1)
|
NP_001334630.1:n.*55T>G
|
|
NM_001347702.1:c.2778T>G
(SYNE1)
|
NP_001334631.1:p.Ala926=
|
|
XM_006715408.2:c.26379T>G
(SYNE1)
|
XP_006715471.1:p.Ala8793=
|
|
XM_006715410.2:c.26349T>G
(SYNE1)
|
XP_006715473.1:p.Ala8783=
|
|
XM_006715412.2:c.26334T>G
(SYNE1)
|
XP_006715475.1:p.Ala8778=
|
|
XM_006715413.2:c.26322T>G
(SYNE1)
|
XP_006715476.1:p.Ala8774=
|
|
XM_006715415.2:c.26280T>G
(SYNE1)
|
XP_006715478.1:p.Ala8760=
|
|
XM_006715416.2:c.26265T>G
(SYNE1)
|
XP_006715479.1:p.Ala8755=
|
|
XM_006715417.2:c.26250T>G
(SYNE1)
|
XP_006715480.1:p.Ala8750=
|
|
XM_006715420.2:c.26238T>G
(SYNE1)
|
XP_006715483.1:p.Ala8746=
|
|
XM_006715421.2:c.26235T>G
(SYNE1)
|
XP_006715484.1:p.Ala8745=
|
|
XM_006715423.2:c.*55T>G
(SYNE1)
|
XP_006715486.1:n.*55T>G
|
|
XM_006715424.2:c.*55T>G
(SYNE1)
|
XP_006715487.1:n.*55T>G
|
|
XM_006715425.2:c.*55T>G
(SYNE1)
|
XP_006715488.1:n.*55T>G
|
|
XM_011535641.2:c.26388T>G
(SYNE1)
|
XP_011533943.1:p.Ala8796=
|
|
XM_011535642.2:c.26376T>G
(SYNE1)
|
XP_011533944.1:p.Ala8792=
|
|
XM_011535645.2:c.24159T>G
(SYNE1)
|
XP_011533947.1:p.Ala8053=
|
|
XM_017010608.1:c.26391T>G
(SYNE1)
|
XP_016866097.1:p.Ala8797=
|
|
XM_017010609.1:c.26391T>G
(SYNE1)
|
XP_016866098.1:p.Ala8797=
|
|
XM_017010610.1:c.26370T>G
(SYNE1)
|
XP_016866099.1:p.Ala8790=
|
|
XM_017010611.2:c.26364T>G
(SYNE1)
|
XP_016866100.1:p.Ala8788=
|
|
XM_017010612.1:c.26313T>G
(SYNE1)
|
XP_016866101.1:p.Ala8771=
|
|
XM_017010613.1:c.26277T>G
(SYNE1)
|
XP_016866102.1:p.Ala8759=
|
|
XM_017010614.1:c.26235T>G
(SYNE1)
|
XP_016866103.1:p.Ala8745=
|
|
XM_017010615.1:c.26124T>G
(SYNE1)
|
XP_016866104.1:p.Ala8708=
|
|
XM_017010616.1:c.*55T>G
(SYNE1)
|
XP_016866105.1:n.*55T>G
|
|
XM_017010617.1:c.*55T>G
(SYNE1)
|
XP_016866106.1:n.*55T>G
|
|
XM_017010618.1:c.*55T>G
(SYNE1)
|
XP_016866107.1:n.*55T>G
|
|
XM_017010619.1:c.24666T>G
(SYNE1)
|
XP_016866108.1:p.Ala8222=
|
|
NM_182961.4:c.26244T>G
(SYNE1)
MANE Select
|
NP_892006.3:p.Ala8748=
|
|
NM_001328100.2:c.851-2680A>C
(ESR1)
|
NP_001315029.1:n.851-2680A>C
|
|
NM_001347701.2:c.*55T>G
(SYNE1)
|
NP_001334630.1:n.*55T>G
|
|
NM_001347702.2:c.2778T>G
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Ala926=
|
|
NM_033071.5:c.26100T>G
(SYNE1)
|
NP_149062.2:p.Ala8700=
|
|