|
ENST00000354674.5:c.2892C>A
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Pro964=
|
|
|
ENST00000367255.10:c.26358C>A
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Pro8786=
|
|
|
ENST00000423061.6:c.26214C>A
(SYNE1)
|
ENSP00000396024.1:p.Pro8738=
|
|
|
ENST00000672154.1:c.1701C>A
(SYNE1)
|
|
|
|
ENST00000672169.1:c.2076C>A
(SYNE1)
|
|
|
|
ENST00000673173.1:c.1943C>A
(SYNE1)
|
|
|
|
ENST00000673451.1:c.2208C>A
(SYNE1)
|
ENSP00000500189.1:n.2208C>A
|
|
|
ENST00000341594.9:c.25143C>A
(SYNE1)
|
ENSP00000341887.6:p.Pro8381=
|
|
|
ENST00000347037.9:n.3106C>A
(SYNE1)
|
|
|
|
ENST00000354674.4:c.2892C>A
(SYNE1)
|
ENSP00000346701.4:p.Pro964=
|
|
|
ENST00000367251.7:c.5134C>A
(SYNE1)
|
ENSP00000356220.3:n.5134C>A
|
|
|
ENST00000367255.9:c.26358C>A
(SYNE1)
|
ENSP00000356224.5:p.Pro8786=
|
|
|
ENST00000367256.9:n.10050C>A
(SYNE1)
|
|
|
|
ENST00000367257.8:c.4237C>A
(SYNE1)
|
ENSP00000356226.4:n.4237C>A
|
|
|
ENST00000409694.6:n.9942C>A
(SYNE1)
|
|
|
|
ENST00000423061.5:c.26214C>A
(SYNE1)
|
ENSP00000396024.1:p.Pro8738=
|
|
|
ENST00000427531.6:c.851-2794G>T
(ESR1)
|
ENSP00000394721.2:n.851-2794G>T
|
|
|
ENST00000460912.6:n.2972C>A
(SYNE1)
|
|
|
|
ENST00000478916.5:n.6995C>A
(SYNE1)
|
|
|
|
ENST00000539504.5:c.2823C>A
(SYNE1)
|
ENSP00000441052.1:p.Pro941=
|
|
|
NM_033071.3:c.26214C>A
(SYNE1)
|
NP_149062.1:p.Pro8738=
|
|
|
NM_182961.3:c.26358C>A
(SYNE1)
|
NP_892006.3:p.Pro8786=
|
|
|
XM_006715407.1:c.26505C>A
(SYNE1)
|
XP_006715470.1:p.Pro8835=
|
|
|
XM_006715408.1:c.26493C>A
(SYNE1)
|
XP_006715471.1:p.Pro8831=
|
|
|
XM_006715409.1:c.26484C>A
(SYNE1)
|
XP_006715472.1:p.Pro8828=
|
|
|
XM_006715410.1:c.26463C>A
(SYNE1)
|
XP_006715473.1:p.Pro8821=
|
|
|
XM_006715411.1:c.26454C>A
(SYNE1)
|
XP_006715474.1:p.Pro8818=
|
|
|
XM_006715412.1:c.26448C>A
(SYNE1)
|
XP_006715475.1:p.Pro8816=
|
|
|
XM_006715413.1:c.26436C>A
(SYNE1)
|
XP_006715476.1:p.Pro8812=
|
|
|
XM_006715414.1:c.26433C>A
(SYNE1)
|
XP_006715477.1:p.Pro8811=
|
|
|
XM_006715415.1:c.26394C>A
(SYNE1)
|
XP_006715478.1:p.Pro8798=
|
|
|
XM_006715416.1:c.26379C>A
(SYNE1)
|
XP_006715479.1:p.Pro8793=
|
|
|
XM_006715417.1:c.26364C>A
(SYNE1)
|
XP_006715480.1:p.Pro8788=
|
|
|
XM_006715420.1:c.26352C>A
(SYNE1)
|
XP_006715483.1:p.Pro8784=
|
|
|
XM_006715421.1:c.26349C>A
(SYNE1)
|
XP_006715484.1:p.Pro8783=
|
|
|
XM_006715422.1:c.26346C>A
(SYNE1)
|
XP_006715485.1:p.Pro8782=
|
|
|
XM_006715423.1:c.*169C>A
(SYNE1)
|
XP_006715486.1:n.*169C>A
|
|
|
XM_006715424.1:c.*169C>A
(SYNE1)
|
XP_006715487.1:n.*169C>A
|
|
|
XM_006715425.1:c.*169C>A
(SYNE1)
|
XP_006715488.1:n.*169C>A
|
|
|
XM_011535641.1:c.26502C>A
(SYNE1)
|
XP_011533943.1:p.Pro8834=
|
|
|
XM_011535642.1:c.26490C>A
(SYNE1)
|
XP_011533944.1:p.Pro8830=
|
|
|
XM_011535643.1:c.26340C>A
(SYNE1)
|
XP_011533945.1:p.Pro8780=
|
|
|
XM_011535644.1:c.24780C>A
(SYNE1)
|
XP_011533946.1:p.Pro8260=
|
|
|
XM_011535645.1:c.24273C>A
(SYNE1)
|
XP_011533947.1:p.Pro8091=
|
|
|
XM_011535647.1:c.19740C>A
(SYNE1)
|
XP_011533949.1:p.Pro6580=
|
|
|
NM_001328100.1:c.851-2794G>T
(ESR1)
|
NP_001315029.1:n.851-2794G>T
|
|
|
NM_001347701.1:c.*169C>A
(SYNE1)
|
NP_001334630.1:n.*169C>A
|
|
|
NM_001347702.1:c.2892C>A
(SYNE1)
|
NP_001334631.1:p.Pro964=
|
|
|
XM_006715408.2:c.26493C>A
(SYNE1)
|
XP_006715471.1:p.Pro8831=
|
|
|
XM_006715410.2:c.26463C>A
(SYNE1)
|
XP_006715473.1:p.Pro8821=
|
|
|
XM_006715412.2:c.26448C>A
(SYNE1)
|
XP_006715475.1:p.Pro8816=
|
|
|
XM_006715413.2:c.26436C>A
(SYNE1)
|
XP_006715476.1:p.Pro8812=
|
|
|
XM_006715415.2:c.26394C>A
(SYNE1)
|
XP_006715478.1:p.Pro8798=
|
|
|
XM_006715416.2:c.26379C>A
(SYNE1)
|
XP_006715479.1:p.Pro8793=
|
|
|
XM_006715417.2:c.26364C>A
(SYNE1)
|
XP_006715480.1:p.Pro8788=
|
|
|
XM_006715420.2:c.26352C>A
(SYNE1)
|
XP_006715483.1:p.Pro8784=
|
|
|
XM_006715421.2:c.26349C>A
(SYNE1)
|
XP_006715484.1:p.Pro8783=
|
|
|
XM_006715423.2:c.*169C>A
(SYNE1)
|
XP_006715486.1:n.*169C>A
|
|
|
XM_006715424.2:c.*169C>A
(SYNE1)
|
XP_006715487.1:n.*169C>A
|
|
|
XM_006715425.2:c.*169C>A
(SYNE1)
|
XP_006715488.1:n.*169C>A
|
|
|
XM_011535641.2:c.26502C>A
(SYNE1)
|
XP_011533943.1:p.Pro8834=
|
|
|
XM_011535642.2:c.26490C>A
(SYNE1)
|
XP_011533944.1:p.Pro8830=
|
|
|
XM_011535645.2:c.24273C>A
(SYNE1)
|
XP_011533947.1:p.Pro8091=
|
|
|
XM_017010608.1:c.26505C>A
(SYNE1)
|
XP_016866097.1:p.Pro8835=
|
|
|
XM_017010609.1:c.26505C>A
(SYNE1)
|
XP_016866098.1:p.Pro8835=
|
|
|
XM_017010610.1:c.26484C>A
(SYNE1)
|
XP_016866099.1:p.Pro8828=
|
|
|
XM_017010611.2:c.26478C>A
(SYNE1)
|
XP_016866100.1:p.Pro8826=
|
|
|
XM_017010612.1:c.26427C>A
(SYNE1)
|
XP_016866101.1:p.Pro8809=
|
|
|
XM_017010613.1:c.26391C>A
(SYNE1)
|
XP_016866102.1:p.Pro8797=
|
|
|
XM_017010614.1:c.26349C>A
(SYNE1)
|
XP_016866103.1:p.Pro8783=
|
|
|
XM_017010615.1:c.26238C>A
(SYNE1)
|
XP_016866104.1:p.Pro8746=
|
|
|
XM_017010616.1:c.*169C>A
(SYNE1)
|
XP_016866105.1:n.*169C>A
|
|
|
XM_017010617.1:c.*169C>A
(SYNE1)
|
XP_016866106.1:n.*169C>A
|
|
|
XM_017010618.1:c.*169C>A
(SYNE1)
|
XP_016866107.1:n.*169C>A
|
|
|
XM_017010619.1:c.24780C>A
(SYNE1)
|
XP_016866108.1:p.Pro8260=
|
|
|
NM_182961.4:c.26358C>A
(SYNE1)
MANE Select
|
NP_892006.3:p.Pro8786=
|
|
|
NM_001328100.2:c.851-2794G>T
(ESR1)
|
NP_001315029.1:n.851-2794G>T
|
|
|
NM_001347701.2:c.*169C>A
(SYNE1)
|
NP_001334630.1:n.*169C>A
|
|
|
NM_001347702.2:c.2892C>A
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Pro964=
|
|
|
NM_033071.5:c.26214C>A
(SYNE1)
|
NP_149062.2:p.Pro8738=
|
|
