|
ENST00000354674.5:c.2914C>T
(SYNE1)
MANE Plus Clinical
|
ENSP00000346701.4:p.Pro972Ser
|
|
|
ENST00000367255.10:c.26380C>T
(SYNE1)
MANE Select
|
ENSP00000356224.5:p.Pro8794Ser
|
|
|
ENST00000423061.6:c.26236C>T
(SYNE1)
|
ENSP00000396024.1:p.Pro8746Ser
|
|
|
ENST00000672154.1:c.1723C>T
(SYNE1)
|
|
|
|
ENST00000672169.1:c.2098C>T
(SYNE1)
|
|
|
|
ENST00000673173.1:c.1965C>T
(SYNE1)
|
|
|
|
ENST00000673451.1:c.2230C>T
(SYNE1)
|
ENSP00000500189.1:n.2230C>T
|
|
|
ENST00000341594.9:c.25165C>T
(SYNE1)
|
ENSP00000341887.6:p.Pro8389Ser
|
|
|
ENST00000347037.9:n.3128C>T
(SYNE1)
|
|
|
|
ENST00000354674.4:c.2914C>T
(SYNE1)
|
ENSP00000346701.4:p.Pro972Ser
|
|
|
ENST00000367251.7:c.5156C>T
(SYNE1)
|
ENSP00000356220.3:n.5156C>T
|
|
|
ENST00000367255.9:c.26380C>T
(SYNE1)
|
ENSP00000356224.5:p.Pro8794Ser
|
|
|
ENST00000367256.9:n.10072C>T
(SYNE1)
|
|
|
|
ENST00000367257.8:c.4259C>T
(SYNE1)
|
ENSP00000356226.4:n.4259C>T
|
|
|
ENST00000409694.6:n.9964C>T
(SYNE1)
|
|
|
|
ENST00000423061.5:c.26236C>T
(SYNE1)
|
ENSP00000396024.1:p.Pro8746Ser
|
|
|
ENST00000427531.6:c.851-2816G>A
(ESR1)
|
ENSP00000394721.2:n.851-2816G>A
|
|
|
ENST00000460912.6:n.2994C>T
(SYNE1)
|
|
|
|
ENST00000478916.5:n.7017C>T
(SYNE1)
|
|
|
|
ENST00000539504.5:c.2845C>T
(SYNE1)
|
ENSP00000441052.1:p.Pro949Ser
|
|
|
NM_033071.3:c.26236C>T
(SYNE1)
|
NP_149062.1:p.Pro8746Ser
|
|
|
NM_182961.3:c.26380C>T
(SYNE1)
|
NP_892006.3:p.Pro8794Ser
|
|
|
XM_006715407.1:c.26527C>T
(SYNE1)
|
XP_006715470.1:p.Pro8843Ser
|
|
|
XM_006715408.1:c.26515C>T
(SYNE1)
|
XP_006715471.1:p.Pro8839Ser
|
|
|
XM_006715409.1:c.26506C>T
(SYNE1)
|
XP_006715472.1:p.Pro8836Ser
|
|
|
XM_006715410.1:c.26485C>T
(SYNE1)
|
XP_006715473.1:p.Pro8829Ser
|
|
|
XM_006715411.1:c.26476C>T
(SYNE1)
|
XP_006715474.1:p.Pro8826Ser
|
|
|
XM_006715412.1:c.26470C>T
(SYNE1)
|
XP_006715475.1:p.Pro8824Ser
|
|
|
XM_006715413.1:c.26458C>T
(SYNE1)
|
XP_006715476.1:p.Pro8820Ser
|
|
|
XM_006715414.1:c.26455C>T
(SYNE1)
|
XP_006715477.1:p.Pro8819Ser
|
|
|
XM_006715415.1:c.26416C>T
(SYNE1)
|
XP_006715478.1:p.Pro8806Ser
|
|
|
XM_006715416.1:c.26401C>T
(SYNE1)
|
XP_006715479.1:p.Pro8801Ser
|
|
|
XM_006715417.1:c.26386C>T
(SYNE1)
|
XP_006715480.1:p.Pro8796Ser
|
|
|
XM_006715420.1:c.26374C>T
(SYNE1)
|
XP_006715483.1:p.Pro8792Ser
|
|
|
XM_006715421.1:c.26371C>T
(SYNE1)
|
XP_006715484.1:p.Pro8791Ser
|
|
|
XM_006715422.1:c.26368C>T
(SYNE1)
|
XP_006715485.1:p.Pro8790Ser
|
|
|
XM_006715423.1:c.*191C>T
(SYNE1)
|
XP_006715486.1:n.*191C>T
|
|
|
XM_006715424.1:c.*191C>T
(SYNE1)
|
XP_006715487.1:n.*191C>T
|
|
|
XM_006715425.1:c.*191C>T
(SYNE1)
|
XP_006715488.1:n.*191C>T
|
|
|
XM_011535641.1:c.26524C>T
(SYNE1)
|
XP_011533943.1:p.Pro8842Ser
|
|
|
XM_011535642.1:c.26512C>T
(SYNE1)
|
XP_011533944.1:p.Pro8838Ser
|
|
|
XM_011535643.1:c.26362C>T
(SYNE1)
|
XP_011533945.1:p.Pro8788Ser
|
|
|
XM_011535644.1:c.24802C>T
(SYNE1)
|
XP_011533946.1:p.Pro8268Ser
|
|
|
XM_011535645.1:c.24295C>T
(SYNE1)
|
XP_011533947.1:p.Pro8099Ser
|
|
|
XM_011535647.1:c.19762C>T
(SYNE1)
|
XP_011533949.1:p.Pro6588Ser
|
|
|
NM_001328100.1:c.851-2816G>A
(ESR1)
|
NP_001315029.1:n.851-2816G>A
|
|
|
NM_001347701.1:c.*191C>T
(SYNE1)
|
NP_001334630.1:n.*191C>T
|
|
|
NM_001347702.1:c.2914C>T
(SYNE1)
|
NP_001334631.1:p.Pro972Ser
|
|
|
XM_006715408.2:c.26515C>T
(SYNE1)
|
XP_006715471.1:p.Pro8839Ser
|
|
|
XM_006715410.2:c.26485C>T
(SYNE1)
|
XP_006715473.1:p.Pro8829Ser
|
|
|
XM_006715412.2:c.26470C>T
(SYNE1)
|
XP_006715475.1:p.Pro8824Ser
|
|
|
XM_006715413.2:c.26458C>T
(SYNE1)
|
XP_006715476.1:p.Pro8820Ser
|
|
|
XM_006715415.2:c.26416C>T
(SYNE1)
|
XP_006715478.1:p.Pro8806Ser
|
|
|
XM_006715416.2:c.26401C>T
(SYNE1)
|
XP_006715479.1:p.Pro8801Ser
|
|
|
XM_006715417.2:c.26386C>T
(SYNE1)
|
XP_006715480.1:p.Pro8796Ser
|
|
|
XM_006715420.2:c.26374C>T
(SYNE1)
|
XP_006715483.1:p.Pro8792Ser
|
|
|
XM_006715421.2:c.26371C>T
(SYNE1)
|
XP_006715484.1:p.Pro8791Ser
|
|
|
XM_006715423.2:c.*191C>T
(SYNE1)
|
XP_006715486.1:n.*191C>T
|
|
|
XM_006715424.2:c.*191C>T
(SYNE1)
|
XP_006715487.1:n.*191C>T
|
|
|
XM_006715425.2:c.*191C>T
(SYNE1)
|
XP_006715488.1:n.*191C>T
|
|
|
XM_011535641.2:c.26524C>T
(SYNE1)
|
XP_011533943.1:p.Pro8842Ser
|
|
|
XM_011535642.2:c.26512C>T
(SYNE1)
|
XP_011533944.1:p.Pro8838Ser
|
|
|
XM_011535645.2:c.24295C>T
(SYNE1)
|
XP_011533947.1:p.Pro8099Ser
|
|
|
XM_017010608.1:c.26527C>T
(SYNE1)
|
XP_016866097.1:p.Pro8843Ser
|
|
|
XM_017010609.1:c.26527C>T
(SYNE1)
|
XP_016866098.1:p.Pro8843Ser
|
|
|
XM_017010610.1:c.26506C>T
(SYNE1)
|
XP_016866099.1:p.Pro8836Ser
|
|
|
XM_017010611.2:c.26500C>T
(SYNE1)
|
XP_016866100.1:p.Pro8834Ser
|
|
|
XM_017010612.1:c.26449C>T
(SYNE1)
|
XP_016866101.1:p.Pro8817Ser
|
|
|
XM_017010613.1:c.26413C>T
(SYNE1)
|
XP_016866102.1:p.Pro8805Ser
|
|
|
XM_017010614.1:c.26371C>T
(SYNE1)
|
XP_016866103.1:p.Pro8791Ser
|
|
|
XM_017010615.1:c.26260C>T
(SYNE1)
|
XP_016866104.1:p.Pro8754Ser
|
|
|
XM_017010616.1:c.*191C>T
(SYNE1)
|
XP_016866105.1:n.*191C>T
|
|
|
XM_017010617.1:c.*191C>T
(SYNE1)
|
XP_016866106.1:n.*191C>T
|
|
|
XM_017010618.1:c.*191C>T
(SYNE1)
|
XP_016866107.1:n.*191C>T
|
|
|
XM_017010619.1:c.24802C>T
(SYNE1)
|
XP_016866108.1:p.Pro8268Ser
|
|
|
NM_182961.4:c.26380C>T
(SYNE1)
MANE Select
|
NP_892006.3:p.Pro8794Ser
|
|
|
NM_001328100.2:c.851-2816G>A
(ESR1)
|
NP_001315029.1:n.851-2816G>A
|
|
|
NM_001347701.2:c.*191C>T
(SYNE1)
|
NP_001334630.1:n.*191C>T
|
|
|
NM_001347702.2:c.2914C>T
(SYNE1)
MANE Plus Clinical
|
NP_001334631.1:p.Pro972Ser
|
|
|
NM_033071.5:c.26236C>T
(SYNE1)
|
NP_149062.2:p.Pro8746Ser
|
|
