|
ENST00000354674.5:c.2799G>C
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Leu933=
|
|
|
ENST00000367255.10:c.26265G>C
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Leu8755=
|
|
|
ENST00000423061.6:c.26121G>C
(SYNE1)
|
ENSP00000396024.1:p.Leu8707=
|
|
|
ENST00000672154.1:c.1608G>C
(SYNE1)
|
|
|
|
ENST00000672169.1:c.1983G>C
(SYNE1)
|
|
|
|
ENST00000673173.1:c.1850G>C
(SYNE1)
|
|
|
|
ENST00000673451.1:c.2115G>C
(SYNE1)
|
ENSP00000500189.1:n.2115G>C
|
|
|
ENST00000341594.9:c.25050G>C
(SYNE1)
|
ENSP00000341887.6:p.Leu8350=
|
|
|
ENST00000347037.9:n.3013G>C
(SYNE1)
|
|
|
|
ENST00000354674.4:c.2799G>C
(SYNE1)
|
ENSP00000346701.4:p.Leu933=
|
|
|
ENST00000367251.7:c.5041G>C
(SYNE1)
|
ENSP00000356220.3:n.5041G>C
|
|
|
ENST00000367255.9:c.26265G>C
(SYNE1)
|
ENSP00000356224.5:p.Leu8755=
|
|
|
ENST00000367256.9:n.9957G>C
(SYNE1)
|
|
|
|
ENST00000367257.8:c.4144G>C
(SYNE1)
|
ENSP00000356226.4:n.4144G>C
|
|
|
ENST00000409694.6:n.9849G>C
(SYNE1)
|
|
|
|
ENST00000423061.5:c.26121G>C
(SYNE1)
|
ENSP00000396024.1:p.Leu8707=
|
|
|
ENST00000427531.6:c.851-2701C>G
(ESR1)
|
ENSP00000394721.2:n.851-2701C>G
|
|
|
ENST00000460912.6:n.2879G>C
(SYNE1)
|
|
|
|
ENST00000478916.5:n.6902G>C
(SYNE1)
|
|
|
|
ENST00000539504.5:c.2730G>C
(SYNE1)
|
ENSP00000441052.1:p.Leu910=
|
|
|
NM_033071.3:c.26121G>C
(SYNE1)
|
NP_149062.1:p.Leu8707=
|
|
|
NM_182961.3:c.26265G>C
(SYNE1)
|
NP_892006.3:p.Leu8755=
|
|
|
XM_006715407.1:c.26412G>C
(SYNE1)
|
XP_006715470.1:p.Leu8804=
|
|
|
XM_006715408.1:c.26400G>C
(SYNE1)
|
XP_006715471.1:p.Leu8800=
|
|
|
XM_006715409.1:c.26391G>C
(SYNE1)
|
XP_006715472.1:p.Leu8797=
|
|
|
XM_006715410.1:c.26370G>C
(SYNE1)
|
XP_006715473.1:p.Leu8790=
|
|
|
XM_006715411.1:c.26361G>C
(SYNE1)
|
XP_006715474.1:p.Leu8787=
|
|
|
XM_006715412.1:c.26355G>C
(SYNE1)
|
XP_006715475.1:p.Leu8785=
|
|
|
XM_006715413.1:c.26343G>C
(SYNE1)
|
XP_006715476.1:p.Leu8781=
|
|
|
XM_006715414.1:c.26340G>C
(SYNE1)
|
XP_006715477.1:p.Leu8780=
|
|
|
XM_006715415.1:c.26301G>C
(SYNE1)
|
XP_006715478.1:p.Leu8767=
|
|
|
XM_006715416.1:c.26286G>C
(SYNE1)
|
XP_006715479.1:p.Leu8762=
|
|
|
XM_006715417.1:c.26271G>C
(SYNE1)
|
XP_006715480.1:p.Leu8757=
|
|
|
XM_006715420.1:c.26259G>C
(SYNE1)
|
XP_006715483.1:p.Leu8753=
|
|
|
XM_006715421.1:c.26256G>C
(SYNE1)
|
XP_006715484.1:p.Leu8752=
|
|
|
XM_006715422.1:c.26253G>C
(SYNE1)
|
XP_006715485.1:p.Leu8751=
|
|
|
XM_006715423.1:c.*76G>C
(SYNE1)
|
XP_006715486.1:n.*76G>C
|
|
|
XM_006715424.1:c.*76G>C
(SYNE1)
|
XP_006715487.1:n.*76G>C
|
|
|
XM_006715425.1:c.*76G>C
(SYNE1)
|
XP_006715488.1:n.*76G>C
|
|
|
XM_011535641.1:c.26409G>C
(SYNE1)
|
XP_011533943.1:p.Leu8803=
|
|
|
XM_011535642.1:c.26397G>C
(SYNE1)
|
XP_011533944.1:p.Leu8799=
|
|
|
XM_011535643.1:c.26247G>C
(SYNE1)
|
XP_011533945.1:p.Leu8749=
|
|
|
XM_011535644.1:c.24687G>C
(SYNE1)
|
XP_011533946.1:p.Leu8229=
|
|
|
XM_011535645.1:c.24180G>C
(SYNE1)
|
XP_011533947.1:p.Leu8060=
|
|
|
XM_011535647.1:c.19647G>C
(SYNE1)
|
XP_011533949.1:p.Leu6549=
|
|
|
NM_001328100.1:c.851-2701C>G
(ESR1)
|
NP_001315029.1:n.851-2701C>G
|
|
|
NM_001347701.1:c.*76G>C
(SYNE1)
|
NP_001334630.1:n.*76G>C
|
|
|
NM_001347702.1:c.2799G>C
(SYNE1)
|
NP_001334631.1:p.Leu933=
|
|
|
XM_006715408.2:c.26400G>C
(SYNE1)
|
XP_006715471.1:p.Leu8800=
|
|
|
XM_006715410.2:c.26370G>C
(SYNE1)
|
XP_006715473.1:p.Leu8790=
|
|
|
XM_006715412.2:c.26355G>C
(SYNE1)
|
XP_006715475.1:p.Leu8785=
|
|
|
XM_006715413.2:c.26343G>C
(SYNE1)
|
XP_006715476.1:p.Leu8781=
|
|
|
XM_006715415.2:c.26301G>C
(SYNE1)
|
XP_006715478.1:p.Leu8767=
|
|
|
XM_006715416.2:c.26286G>C
(SYNE1)
|
XP_006715479.1:p.Leu8762=
|
|
|
XM_006715417.2:c.26271G>C
(SYNE1)
|
XP_006715480.1:p.Leu8757=
|
|
|
XM_006715420.2:c.26259G>C
(SYNE1)
|
XP_006715483.1:p.Leu8753=
|
|
|
XM_006715421.2:c.26256G>C
(SYNE1)
|
XP_006715484.1:p.Leu8752=
|
|
|
XM_006715423.2:c.*76G>C
(SYNE1)
|
XP_006715486.1:n.*76G>C
|
|
|
XM_006715424.2:c.*76G>C
(SYNE1)
|
XP_006715487.1:n.*76G>C
|
|
|
XM_006715425.2:c.*76G>C
(SYNE1)
|
XP_006715488.1:n.*76G>C
|
|
|
XM_011535641.2:c.26409G>C
(SYNE1)
|
XP_011533943.1:p.Leu8803=
|
|
|
XM_011535642.2:c.26397G>C
(SYNE1)
|
XP_011533944.1:p.Leu8799=
|
|
|
XM_011535645.2:c.24180G>C
(SYNE1)
|
XP_011533947.1:p.Leu8060=
|
|
|
XM_017010608.1:c.26412G>C
(SYNE1)
|
XP_016866097.1:p.Leu8804=
|
|
|
XM_017010609.1:c.26412G>C
(SYNE1)
|
XP_016866098.1:p.Leu8804=
|
|
|
XM_017010610.1:c.26391G>C
(SYNE1)
|
XP_016866099.1:p.Leu8797=
|
|
|
XM_017010611.2:c.26385G>C
(SYNE1)
|
XP_016866100.1:p.Leu8795=
|
|
|
XM_017010612.1:c.26334G>C
(SYNE1)
|
XP_016866101.1:p.Leu8778=
|
|
|
XM_017010613.1:c.26298G>C
(SYNE1)
|
XP_016866102.1:p.Leu8766=
|
|
|
XM_017010614.1:c.26256G>C
(SYNE1)
|
XP_016866103.1:p.Leu8752=
|
|
|
XM_017010615.1:c.26145G>C
(SYNE1)
|
XP_016866104.1:p.Leu8715=
|
|
|
XM_017010616.1:c.*76G>C
(SYNE1)
|
XP_016866105.1:n.*76G>C
|
|
|
XM_017010617.1:c.*76G>C
(SYNE1)
|
XP_016866106.1:n.*76G>C
|
|
|
XM_017010618.1:c.*76G>C
(SYNE1)
|
XP_016866107.1:n.*76G>C
|
|
|
XM_017010619.1:c.24687G>C
(SYNE1)
|
XP_016866108.1:p.Leu8229=
|
|
|
NM_182961.4:c.26265G>C
(SYNE1)
MANE Select
|
NP_892006.3:p.Leu8755=
|
|
|
NM_001328100.2:c.851-2701C>G
(ESR1)
|
NP_001315029.1:n.851-2701C>G
|
|
|
NM_001347701.2:c.*76G>C
(SYNE1)
|
NP_001334630.1:n.*76G>C
|
|
|
NM_001347702.2:c.2799G>C
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Leu933=
|
|
|
NM_033071.5:c.26121G>C
(SYNE1)
|
NP_149062.2:p.Leu8707=
|
|
