ENST00000555002.6:c.14237G>A
(SYNE2)
MANE Select
|
ENSP00000450831.2:p.Gly4746Asp
|
|
ENST00000673797.1:c.1640G>A
(SYNE2)
|
ENSP00000501238.1:p.Gly547Asp
|
|
ENST00000344113.8:c.14237G>A
(SYNE2)
|
ENSP00000341781.4:p.Gly4746Asp
|
|
ENST00000357395.7:c.13988G>A
(SYNE2)
|
ENSP00000349969.4:p.Gly4663Asp
|
|
ENST00000358025.7:c.14237G>A
(SYNE2)
|
ENSP00000350719.3:p.Gly4746Asp
|
|
ENST00000394768.6:c.3392G>A
(SYNE2)
|
ENSP00000378249.2:p.Gly1131Asp
|
|
ENST00000554584.5:c.13988G>A
(SYNE2)
|
ENSP00000452570.1:p.Gly4663Asp
|
|
ENST00000555002.5:c.4139G>A
(SYNE2)
|
ENSP00000450831.1:p.Gly1380Asp
|
|
ENST00000556275.5:c.1407-45093C>T
(ESR2)
|
ENSP00000452485.2:n.1407-45093C>T
|
|
NM_015180.4:c.14237G>A
(SYNE2)
|
NP_055995.4:p.Gly4746Asp
|
|
NM_182914.2:c.14237G>A
(SYNE2)
|
NP_878918.2:p.Gly4746Asp
|
|
XM_005267454.1:c.14237G>A
(SYNE2)
|
XP_005267511.1:p.Gly4746Asp
|
|
XM_005267456.1:c.14237G>A
(SYNE2)
|
XP_005267513.1:p.Gly4746Asp
|
|
XM_005267457.1:c.14237G>A
(SYNE2)
|
XP_005267514.1:p.Gly4746Asp
|
|
XM_005267458.1:c.14237G>A
(SYNE2)
|
XP_005267515.1:p.Gly4746Asp
|
|
XM_005267459.1:c.14237G>A
(SYNE2)
|
XP_005267516.1:p.Gly4746Asp
|
|
XM_006720084.2:c.14237G>A
(SYNE2)
|
XP_006720147.1:p.Gly4746Asp
|
|
XM_011536574.1:c.14237G>A
(SYNE2)
|
XP_011534876.1:p.Gly4746Asp
|
|
XM_011536575.1:c.14237G>A
(SYNE2)
|
XP_011534877.1:p.Gly4746Asp
|
|
XM_011536576.1:c.14237G>A
(SYNE2)
|
XP_011534878.1:p.Gly4746Asp
|
|
XM_011536577.1:c.14237G>A
(SYNE2)
|
XP_011534879.1:p.Gly4746Asp
|
|
XM_011536578.1:c.14237G>A
(SYNE2)
|
XP_011534880.1:p.Gly4746Asp
|
|
XM_011536579.1:c.14237G>A
(SYNE2)
|
XP_011534881.1:p.Gly4746Asp
|
|
XM_011536580.1:c.14237G>A
(SYNE2)
|
XP_011534882.1:p.Gly4746Asp
|
|
XM_011536581.1:c.14237G>A
(SYNE2)
|
XP_011534883.1:p.Gly4746Asp
|
|
XM_011536582.1:c.14120G>A
(SYNE2)
|
XP_011534884.1:p.Gly4707Asp
|
|
XM_011536583.1:c.11042G>A
(SYNE2)
|
XP_011534885.1:p.Gly3681Asp
|
|
XM_011536575.2:c.14237G>A
(SYNE2)
|
XP_011534877.1:p.Gly4746Asp
|
|
XM_011536576.2:c.14237G>A
(SYNE2)
|
XP_011534878.1:p.Gly4746Asp
|
|
XM_011536577.2:c.14237G>A
(SYNE2)
|
XP_011534879.1:p.Gly4746Asp
|
|
XM_011536580.2:c.14237G>A
(SYNE2)
|
XP_011534882.1:p.Gly4746Asp
|
|
XM_017021101.1:c.14237G>A
(SYNE2)
|
XP_016876590.1:p.Gly4746Asp
|
|
XM_017021102.1:c.14168G>A
(SYNE2)
|
XP_016876591.1:p.Gly4723Asp
|
|
XR_001750198.1:n.14467G>A
(SYNE2)
|
|
|
NM_015180.5:c.14237G>A
(SYNE2)
|
NP_055995.4:p.Gly4746Asp
|
|
NM_015180.6:c.14237G>A
(SYNE2)
|
NP_055995.4:p.Gly4746Asp
|
|
NM_182914.3:c.14237G>A
(SYNE2)
MANE Select
|
NP_878918.2:p.Gly4746Asp
|
|