ENST00000371375.2:c.5457G>T
(PLCE1)
|
ENSP00000360426.1:p.Glu1819Asp
|
|
ENST00000685132.1:n.3780G>T
(PLCE1)
|
|
|
ENST00000685253.1:c.*2924G>T
(PLCE1)
|
ENSP00000509405.1:n.*2924G>T
|
|
ENST00000685889.1:n.3116G>T
(PLCE1)
|
|
|
ENST00000686807.1:n.1800G>T
(PLCE1)
|
|
|
ENST00000686954.1:c.*1665G>T
(PLCE1)
|
ENSP00000508416.1:n.*1665G>T
|
|
ENST00000688810.1:c.5409G>T
(PLCE1)
|
ENSP00000509140.1:p.Glu1803Asp
|
|
ENST00000689233.1:n.10589G>T
(PLCE1)
|
|
|
ENST00000690340.1:n.4054G>T
(PLCE1)
|
|
|
ENST00000692286.1:c.6249G>T
(PLCE1)
|
ENSP00000509490.1:p.Glu2083Asp
|
|
ENST00000692396.1:c.6333G>T
(PLCE1)
|
ENSP00000508605.1:p.Glu2111Asp
|
|
ENST00000371380.8:c.6381G>T
(PLCE1)
MANE Select
|
ENSP00000360431.2:p.Glu2127Asp
|
|
ENST00000371385.8:c.5355G>T
(PLCE1)
|
ENSP00000360438.4:p.Glu1785Asp
|
|
ENST00000674738.1:c.4936G>T
(PLCE1)
|
|
|
ENST00000674827.1:c.4497G>T
(PLCE1)
|
ENSP00000502523.1:p.Glu1499Asp
|
|
ENST00000675218.1:c.5457G>T
(PLCE1)
|
ENSP00000501910.1:p.Glu1819Asp
|
|
ENST00000675487.1:c.*2314G>T
(PLCE1)
|
ENSP00000502340.1:n.*2314G>T
|
|
ENST00000675718.1:c.5650G>T
(PLCE1)
|
|
|
ENST00000260766.7:c.6381G>T
(PLCE1)
|
ENSP00000260766.3:p.Glu2127Asp
|
|
ENST00000371375.1:c.5457G>T
(PLCE1)
|
ENSP00000360426.1:p.Glu1819Asp
|
|
ENST00000371380.7:c.6381G>T
(PLCE1)
|
ENSP00000360431.2:p.Glu2127Asp
|
|
ENST00000371385.7:c.5457G>T
(PLCE1)
|
ENSP00000360438.3:p.Glu1819Asp
|
|
NM_001165979.2:c.5457G>T
(PLCE1)
|
NP_001159451.1:p.Glu1819Asp
|
|
NM_001288989.1:c.6333G>T
(PLCE1)
|
NP_001275918.1:p.Glu2111Asp
|
|
NM_016341.3:c.6381G>T
(PLCE1)
|
NP_057425.3:p.Glu2127Asp
|
|
XM_006717885.2:c.6423G>T
(PLCE1)
|
XP_006717948.1:p.Glu2141Asp
|
|
XM_006717886.2:c.6423G>T
(PLCE1)
|
XP_006717949.1:p.Glu2141Asp
|
|
XM_006717888.2:c.6420G>T
(PLCE1)
|
XP_006717951.1:p.Glu2140Asp
|
|
XM_006717889.2:c.6375G>T
(PLCE1)
|
XP_006717952.1:p.Glu2125Asp
|
|
XM_006717890.1:c.5499G>T
(PLCE1)
|
XP_006717953.1:p.Glu1833Asp
|
|
XM_011539849.1:c.6423G>T
(PLCE1)
|
XP_011538151.1:p.Glu2141Asp
|
|
XM_011539850.1:c.5268G>T
(PLCE1)
|
XP_011538152.1:p.Glu1756Asp
|
|
XR_945799.1:n.3311-6475C>A
(NOC3L)
|
|
|
XM_006717885.4:c.6423G>T
(PLCE1)
|
XP_006717948.1:p.Glu2141Asp
|
|
XM_006717888.4:c.6420G>T
(PLCE1)
|
XP_006717951.1:p.Glu2140Asp
|
|
XM_006717889.4:c.6375G>T
(PLCE1)
|
XP_006717952.1:p.Glu2125Asp
|
|
XM_006717890.3:c.5499G>T
(PLCE1)
|
XP_006717953.1:p.Glu1833Asp
|
|
XM_011539849.3:c.6423G>T
(PLCE1)
|
XP_011538151.1:p.Glu2141Asp
|
|
XM_011539850.3:c.5268G>T
(PLCE1)
|
XP_011538152.1:p.Glu1756Asp
|
|
XM_017016310.2:c.6423G>T
(PLCE1)
|
XP_016871799.1:p.Glu2141Asp
|
|
XM_017016311.2:c.6423G>T
(PLCE1)
|
XP_016871800.1:p.Glu2141Asp
|
|
XM_017016312.2:c.5409G>T
(PLCE1)
|
XP_016871801.1:p.Glu1803Asp
|
|
XR_002957007.1:n.3312-6475C>A
(NOC3L)
|
|
|
NM_001288989.2:c.6333G>T
(PLCE1)
|
NP_001275918.1:p.Glu2111Asp
|
|
NM_016341.4:c.6381G>T
(PLCE1)
MANE Select
|
NP_057425.3:p.Glu2127Asp
|
|