|
ENST00000354674.5:c.2900G>C
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Arg967Thr
|
|
|
ENST00000367255.10:c.26366G>C
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Arg8789Thr
|
|
|
ENST00000423061.6:c.26222G>C
(SYNE1)
|
ENSP00000396024.1:p.Arg8741Thr
|
|
|
ENST00000672154.1:c.1709G>C
(SYNE1)
|
|
|
|
ENST00000672169.1:c.2084G>C
(SYNE1)
|
|
|
|
ENST00000673173.1:c.1951G>C
(SYNE1)
|
|
|
|
ENST00000673451.1:c.2216G>C
(SYNE1)
|
ENSP00000500189.1:n.2216G>C
|
|
|
ENST00000341594.9:c.25151G>C
(SYNE1)
|
ENSP00000341887.6:p.Arg8384Thr
|
|
|
ENST00000347037.9:n.3114G>C
(SYNE1)
|
|
|
|
ENST00000354674.4:c.2900G>C
(SYNE1)
|
ENSP00000346701.4:p.Arg967Thr
|
|
|
ENST00000367251.7:c.5142G>C
(SYNE1)
|
ENSP00000356220.3:n.5142G>C
|
|
|
ENST00000367255.9:c.26366G>C
(SYNE1)
|
ENSP00000356224.5:p.Arg8789Thr
|
|
|
ENST00000367256.9:n.10058G>C
(SYNE1)
|
|
|
|
ENST00000367257.8:c.4245G>C
(SYNE1)
|
ENSP00000356226.4:n.4245G>C
|
|
|
ENST00000409694.6:n.9950G>C
(SYNE1)
|
|
|
|
ENST00000423061.5:c.26222G>C
(SYNE1)
|
ENSP00000396024.1:p.Arg8741Thr
|
|
|
ENST00000427531.6:c.851-2802C>G
(ESR1)
|
ENSP00000394721.2:n.851-2802C>G
|
|
|
ENST00000460912.6:n.2980G>C
(SYNE1)
|
|
|
|
ENST00000478916.5:n.7003G>C
(SYNE1)
|
|
|
|
ENST00000539504.5:c.2831G>C
(SYNE1)
|
ENSP00000441052.1:p.Arg944Thr
|
|
|
NM_033071.3:c.26222G>C
(SYNE1)
|
NP_149062.1:p.Arg8741Thr
|
|
|
NM_182961.3:c.26366G>C
(SYNE1)
|
NP_892006.3:p.Arg8789Thr
|
|
|
XM_006715407.1:c.26513G>C
(SYNE1)
|
XP_006715470.1:p.Arg8838Thr
|
|
|
XM_006715408.1:c.26501G>C
(SYNE1)
|
XP_006715471.1:p.Arg8834Thr
|
|
|
XM_006715409.1:c.26492G>C
(SYNE1)
|
XP_006715472.1:p.Arg8831Thr
|
|
|
XM_006715410.1:c.26471G>C
(SYNE1)
|
XP_006715473.1:p.Arg8824Thr
|
|
|
XM_006715411.1:c.26462G>C
(SYNE1)
|
XP_006715474.1:p.Arg8821Thr
|
|
|
XM_006715412.1:c.26456G>C
(SYNE1)
|
XP_006715475.1:p.Arg8819Thr
|
|
|
XM_006715413.1:c.26444G>C
(SYNE1)
|
XP_006715476.1:p.Arg8815Thr
|
|
|
XM_006715414.1:c.26441G>C
(SYNE1)
|
XP_006715477.1:p.Arg8814Thr
|
|
|
XM_006715415.1:c.26402G>C
(SYNE1)
|
XP_006715478.1:p.Arg8801Thr
|
|
|
XM_006715416.1:c.26387G>C
(SYNE1)
|
XP_006715479.1:p.Arg8796Thr
|
|
|
XM_006715417.1:c.26372G>C
(SYNE1)
|
XP_006715480.1:p.Arg8791Thr
|
|
|
XM_006715420.1:c.26360G>C
(SYNE1)
|
XP_006715483.1:p.Arg8787Thr
|
|
|
XM_006715421.1:c.26357G>C
(SYNE1)
|
XP_006715484.1:p.Arg8786Thr
|
|
|
XM_006715422.1:c.26354G>C
(SYNE1)
|
XP_006715485.1:p.Arg8785Thr
|
|
|
XM_006715423.1:c.*177G>C
(SYNE1)
|
XP_006715486.1:n.*177G>C
|
|
|
XM_006715424.1:c.*177G>C
(SYNE1)
|
XP_006715487.1:n.*177G>C
|
|
|
XM_006715425.1:c.*177G>C
(SYNE1)
|
XP_006715488.1:n.*177G>C
|
|
|
XM_011535641.1:c.26510G>C
(SYNE1)
|
XP_011533943.1:p.Arg8837Thr
|
|
|
XM_011535642.1:c.26498G>C
(SYNE1)
|
XP_011533944.1:p.Arg8833Thr
|
|
|
XM_011535643.1:c.26348G>C
(SYNE1)
|
XP_011533945.1:p.Arg8783Thr
|
|
|
XM_011535644.1:c.24788G>C
(SYNE1)
|
XP_011533946.1:p.Arg8263Thr
|
|
|
XM_011535645.1:c.24281G>C
(SYNE1)
|
XP_011533947.1:p.Arg8094Thr
|
|
|
XM_011535647.1:c.19748G>C
(SYNE1)
|
XP_011533949.1:p.Arg6583Thr
|
|
|
NM_001328100.1:c.851-2802C>G
(ESR1)
|
NP_001315029.1:n.851-2802C>G
|
|
|
NM_001347701.1:c.*177G>C
(SYNE1)
|
NP_001334630.1:n.*177G>C
|
|
|
NM_001347702.1:c.2900G>C
(SYNE1)
|
NP_001334631.1:p.Arg967Thr
|
|
|
XM_006715408.2:c.26501G>C
(SYNE1)
|
XP_006715471.1:p.Arg8834Thr
|
|
|
XM_006715410.2:c.26471G>C
(SYNE1)
|
XP_006715473.1:p.Arg8824Thr
|
|
|
XM_006715412.2:c.26456G>C
(SYNE1)
|
XP_006715475.1:p.Arg8819Thr
|
|
|
XM_006715413.2:c.26444G>C
(SYNE1)
|
XP_006715476.1:p.Arg8815Thr
|
|
|
XM_006715415.2:c.26402G>C
(SYNE1)
|
XP_006715478.1:p.Arg8801Thr
|
|
|
XM_006715416.2:c.26387G>C
(SYNE1)
|
XP_006715479.1:p.Arg8796Thr
|
|
|
XM_006715417.2:c.26372G>C
(SYNE1)
|
XP_006715480.1:p.Arg8791Thr
|
|
|
XM_006715420.2:c.26360G>C
(SYNE1)
|
XP_006715483.1:p.Arg8787Thr
|
|
|
XM_006715421.2:c.26357G>C
(SYNE1)
|
XP_006715484.1:p.Arg8786Thr
|
|
|
XM_006715423.2:c.*177G>C
(SYNE1)
|
XP_006715486.1:n.*177G>C
|
|
|
XM_006715424.2:c.*177G>C
(SYNE1)
|
XP_006715487.1:n.*177G>C
|
|
|
XM_006715425.2:c.*177G>C
(SYNE1)
|
XP_006715488.1:n.*177G>C
|
|
|
XM_011535641.2:c.26510G>C
(SYNE1)
|
XP_011533943.1:p.Arg8837Thr
|
|
|
XM_011535642.2:c.26498G>C
(SYNE1)
|
XP_011533944.1:p.Arg8833Thr
|
|
|
XM_011535645.2:c.24281G>C
(SYNE1)
|
XP_011533947.1:p.Arg8094Thr
|
|
|
XM_017010608.1:c.26513G>C
(SYNE1)
|
XP_016866097.1:p.Arg8838Thr
|
|
|
XM_017010609.1:c.26513G>C
(SYNE1)
|
XP_016866098.1:p.Arg8838Thr
|
|
|
XM_017010610.1:c.26492G>C
(SYNE1)
|
XP_016866099.1:p.Arg8831Thr
|
|
|
XM_017010611.2:c.26486G>C
(SYNE1)
|
XP_016866100.1:p.Arg8829Thr
|
|
|
XM_017010612.1:c.26435G>C
(SYNE1)
|
XP_016866101.1:p.Arg8812Thr
|
|
|
XM_017010613.1:c.26399G>C
(SYNE1)
|
XP_016866102.1:p.Arg8800Thr
|
|
|
XM_017010614.1:c.26357G>C
(SYNE1)
|
XP_016866103.1:p.Arg8786Thr
|
|
|
XM_017010615.1:c.26246G>C
(SYNE1)
|
XP_016866104.1:p.Arg8749Thr
|
|
|
XM_017010616.1:c.*177G>C
(SYNE1)
|
XP_016866105.1:n.*177G>C
|
|
|
XM_017010617.1:c.*177G>C
(SYNE1)
|
XP_016866106.1:n.*177G>C
|
|
|
XM_017010618.1:c.*177G>C
(SYNE1)
|
XP_016866107.1:n.*177G>C
|
|
|
XM_017010619.1:c.24788G>C
(SYNE1)
|
XP_016866108.1:p.Arg8263Thr
|
|
|
NM_182961.4:c.26366G>C
(SYNE1)
MANE Select
|
NP_892006.3:p.Arg8789Thr
|
|
|
NM_001328100.2:c.851-2802C>G
(ESR1)
|
NP_001315029.1:n.851-2802C>G
|
|
|
NM_001347701.2:c.*177G>C
(SYNE1)
|
NP_001334630.1:n.*177G>C
|
|
|
NM_001347702.2:c.2900G>C
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Arg967Thr
|
|
|
NM_033071.5:c.26222G>C
(SYNE1)
|
NP_149062.2:p.Arg8741Thr
|
|
