ENST00000354674.5:c.2785C>T
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Leu929Phe
|
|
ENST00000367255.10:c.26251C>T
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Leu8751Phe
|
|
ENST00000423061.6:c.26107C>T
(SYNE1)
|
ENSP00000396024.1:p.Leu8703Phe
|
|
ENST00000672154.1:c.1594C>T
(SYNE1)
|
|
|
ENST00000672169.1:c.1969C>T
(SYNE1)
|
|
|
ENST00000673173.1:c.1836C>T
(SYNE1)
|
|
|
ENST00000673451.1:c.2101C>T
(SYNE1)
|
ENSP00000500189.1:n.2101C>T
|
|
ENST00000341594.9:c.25036C>T
(SYNE1)
|
ENSP00000341887.6:p.Leu8346Phe
|
|
ENST00000347037.9:n.2999C>T
(SYNE1)
|
|
|
ENST00000354674.4:c.2785C>T
(SYNE1)
|
ENSP00000346701.4:p.Leu929Phe
|
|
ENST00000367251.7:c.5027C>T
(SYNE1)
|
ENSP00000356220.3:n.5027C>T
|
|
ENST00000367255.9:c.26251C>T
(SYNE1)
|
ENSP00000356224.5:p.Leu8751Phe
|
|
ENST00000367256.9:n.9943C>T
(SYNE1)
|
|
|
ENST00000367257.8:c.4130C>T
(SYNE1)
|
ENSP00000356226.4:n.4130C>T
|
|
ENST00000409694.6:n.9835C>T
(SYNE1)
|
|
|
ENST00000423061.5:c.26107C>T
(SYNE1)
|
ENSP00000396024.1:p.Leu8703Phe
|
|
ENST00000427531.6:c.851-2687G>A
(ESR1)
|
ENSP00000394721.2:n.851-2687G>A
|
|
ENST00000460912.6:n.2865C>T
(SYNE1)
|
|
|
ENST00000478916.5:n.6888C>T
(SYNE1)
|
|
|
ENST00000539504.5:c.2716C>T
(SYNE1)
|
ENSP00000441052.1:p.Leu906Phe
|
|
NM_033071.3:c.26107C>T
(SYNE1)
|
NP_149062.1:p.Leu8703Phe
|
|
NM_182961.3:c.26251C>T
(SYNE1)
|
NP_892006.3:p.Leu8751Phe
|
|
XM_006715407.1:c.26398C>T
(SYNE1)
|
XP_006715470.1:p.Leu8800Phe
|
|
XM_006715408.1:c.26386C>T
(SYNE1)
|
XP_006715471.1:p.Leu8796Phe
|
|
XM_006715409.1:c.26377C>T
(SYNE1)
|
XP_006715472.1:p.Leu8793Phe
|
|
XM_006715410.1:c.26356C>T
(SYNE1)
|
XP_006715473.1:p.Leu8786Phe
|
|
XM_006715411.1:c.26347C>T
(SYNE1)
|
XP_006715474.1:p.Leu8783Phe
|
|
XM_006715412.1:c.26341C>T
(SYNE1)
|
XP_006715475.1:p.Leu8781Phe
|
|
XM_006715413.1:c.26329C>T
(SYNE1)
|
XP_006715476.1:p.Leu8777Phe
|
|
XM_006715414.1:c.26326C>T
(SYNE1)
|
XP_006715477.1:p.Leu8776Phe
|
|
XM_006715415.1:c.26287C>T
(SYNE1)
|
XP_006715478.1:p.Leu8763Phe
|
|
XM_006715416.1:c.26272C>T
(SYNE1)
|
XP_006715479.1:p.Leu8758Phe
|
|
XM_006715417.1:c.26257C>T
(SYNE1)
|
XP_006715480.1:p.Leu8753Phe
|
|
XM_006715420.1:c.26245C>T
(SYNE1)
|
XP_006715483.1:p.Leu8749Phe
|
|
XM_006715421.1:c.26242C>T
(SYNE1)
|
XP_006715484.1:p.Leu8748Phe
|
|
XM_006715422.1:c.26239C>T
(SYNE1)
|
XP_006715485.1:p.Leu8747Phe
|
|
XM_006715423.1:c.*62C>T
(SYNE1)
|
XP_006715486.1:n.*62C>T
|
|
XM_006715424.1:c.*62C>T
(SYNE1)
|
XP_006715487.1:n.*62C>T
|
|
XM_006715425.1:c.*62C>T
(SYNE1)
|
XP_006715488.1:n.*62C>T
|
|
XM_011535641.1:c.26395C>T
(SYNE1)
|
XP_011533943.1:p.Leu8799Phe
|
|
XM_011535642.1:c.26383C>T
(SYNE1)
|
XP_011533944.1:p.Leu8795Phe
|
|
XM_011535643.1:c.26233C>T
(SYNE1)
|
XP_011533945.1:p.Leu8745Phe
|
|
XM_011535644.1:c.24673C>T
(SYNE1)
|
XP_011533946.1:p.Leu8225Phe
|
|
XM_011535645.1:c.24166C>T
(SYNE1)
|
XP_011533947.1:p.Leu8056Phe
|
|
XM_011535647.1:c.19633C>T
(SYNE1)
|
XP_011533949.1:p.Leu6545Phe
|
|
NM_001328100.1:c.851-2687G>A
(ESR1)
|
NP_001315029.1:n.851-2687G>A
|
|
NM_001347701.1:c.*62C>T
(SYNE1)
|
NP_001334630.1:n.*62C>T
|
|
NM_001347702.1:c.2785C>T
(SYNE1)
|
NP_001334631.1:p.Leu929Phe
|
|
XM_006715408.2:c.26386C>T
(SYNE1)
|
XP_006715471.1:p.Leu8796Phe
|
|
XM_006715410.2:c.26356C>T
(SYNE1)
|
XP_006715473.1:p.Leu8786Phe
|
|
XM_006715412.2:c.26341C>T
(SYNE1)
|
XP_006715475.1:p.Leu8781Phe
|
|
XM_006715413.2:c.26329C>T
(SYNE1)
|
XP_006715476.1:p.Leu8777Phe
|
|
XM_006715415.2:c.26287C>T
(SYNE1)
|
XP_006715478.1:p.Leu8763Phe
|
|
XM_006715416.2:c.26272C>T
(SYNE1)
|
XP_006715479.1:p.Leu8758Phe
|
|
XM_006715417.2:c.26257C>T
(SYNE1)
|
XP_006715480.1:p.Leu8753Phe
|
|
XM_006715420.2:c.26245C>T
(SYNE1)
|
XP_006715483.1:p.Leu8749Phe
|
|
XM_006715421.2:c.26242C>T
(SYNE1)
|
XP_006715484.1:p.Leu8748Phe
|
|
XM_006715423.2:c.*62C>T
(SYNE1)
|
XP_006715486.1:n.*62C>T
|
|
XM_006715424.2:c.*62C>T
(SYNE1)
|
XP_006715487.1:n.*62C>T
|
|
XM_006715425.2:c.*62C>T
(SYNE1)
|
XP_006715488.1:n.*62C>T
|
|
XM_011535641.2:c.26395C>T
(SYNE1)
|
XP_011533943.1:p.Leu8799Phe
|
|
XM_011535642.2:c.26383C>T
(SYNE1)
|
XP_011533944.1:p.Leu8795Phe
|
|
XM_011535645.2:c.24166C>T
(SYNE1)
|
XP_011533947.1:p.Leu8056Phe
|
|
XM_017010608.1:c.26398C>T
(SYNE1)
|
XP_016866097.1:p.Leu8800Phe
|
|
XM_017010609.1:c.26398C>T
(SYNE1)
|
XP_016866098.1:p.Leu8800Phe
|
|
XM_017010610.1:c.26377C>T
(SYNE1)
|
XP_016866099.1:p.Leu8793Phe
|
|
XM_017010611.2:c.26371C>T
(SYNE1)
|
XP_016866100.1:p.Leu8791Phe
|
|
XM_017010612.1:c.26320C>T
(SYNE1)
|
XP_016866101.1:p.Leu8774Phe
|
|
XM_017010613.1:c.26284C>T
(SYNE1)
|
XP_016866102.1:p.Leu8762Phe
|
|
XM_017010614.1:c.26242C>T
(SYNE1)
|
XP_016866103.1:p.Leu8748Phe
|
|
XM_017010615.1:c.26131C>T
(SYNE1)
|
XP_016866104.1:p.Leu8711Phe
|
|
XM_017010616.1:c.*62C>T
(SYNE1)
|
XP_016866105.1:n.*62C>T
|
|
XM_017010617.1:c.*62C>T
(SYNE1)
|
XP_016866106.1:n.*62C>T
|
|
XM_017010618.1:c.*62C>T
(SYNE1)
|
XP_016866107.1:n.*62C>T
|
|
XM_017010619.1:c.24673C>T
(SYNE1)
|
XP_016866108.1:p.Leu8225Phe
|
|
NM_182961.4:c.26251C>T
(SYNE1)
MANE Select
|
NP_892006.3:p.Leu8751Phe
|
|
NM_001328100.2:c.851-2687G>A
(ESR1)
|
NP_001315029.1:n.851-2687G>A
|
|
NM_001347701.2:c.*62C>T
(SYNE1)
|
NP_001334630.1:n.*62C>T
|
|
NM_001347702.2:c.2785C>T
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Leu929Phe
|
|
NM_033071.5:c.26107C>T
(SYNE1)
|
NP_149062.2:p.Leu8703Phe
|
|