|
ENST00000371375.2:c.3748C>T
(PLCE1)
|
ENSP00000360426.1:p.Gln1250Ter
|
|
|
ENST00000685253.1:c.*1215C>T
(PLCE1)
|
ENSP00000509405.1:n.*1215C>T
|
|
|
ENST00000685889.1:n.1407C>T
(PLCE1)
|
|
|
|
ENST00000686954.1:c.4672C>T
(PLCE1)
|
ENSP00000508416.1:p.Gln1558Ter
|
|
|
ENST00000688810.1:c.3700C>T
(PLCE1)
|
ENSP00000509140.1:p.Gln1234Ter
|
|
|
ENST00000689233.1:n.5002C>T
(PLCE1)
|
|
|
|
ENST00000692286.1:c.4672C>T
(PLCE1)
|
ENSP00000509490.1:p.Gln1558Ter
|
|
|
ENST00000692396.1:c.4624C>T
(PLCE1)
|
ENSP00000508605.1:p.Gln1542Ter
|
|
|
ENST00000371380.8:c.4672C>T
(PLCE1)
MANE Select
|
ENSP00000360431.2:p.Gln1558Ter
|
|
|
ENST00000371385.8:c.3646C>T
(PLCE1)
|
ENSP00000360438.4:p.Gln1216Ter
|
|
|
ENST00000674738.1:c.3077C>T
(PLCE1)
|
|
|
|
ENST00000674827.1:c.2749C>T
(PLCE1)
|
ENSP00000502523.1:p.Gln917Ter
|
|
|
ENST00000675218.1:c.3748C>T
(PLCE1)
|
ENSP00000501910.1:p.Gln1250Ter
|
|
|
ENST00000675487.1:c.*605C>T
(PLCE1)
|
ENSP00000502340.1:n.*605C>T
|
|
|
ENST00000675718.1:c.3899C>T
(PLCE1)
|
|
|
|
ENST00000676102.1:c.3517C>T
(PLCE1)
|
ENSP00000502811.1:p.Gln1173Ter
|
|
|
ENST00000260766.7:c.4672C>T
(PLCE1)
|
ENSP00000260766.3:p.Gln1558Ter
|
|
|
ENST00000371375.1:c.3748C>T
(PLCE1)
|
ENSP00000360426.1:p.Gln1250Ter
|
|
|
ENST00000371380.7:c.4672C>T
(PLCE1)
|
ENSP00000360431.2:p.Gln1558Ter
|
|
|
ENST00000371385.7:c.3748C>T
(PLCE1)
|
ENSP00000360438.3:p.Gln1250Ter
|
|
|
NM_001165979.2:c.3748C>T
(PLCE1)
|
NP_001159451.1:p.Gln1250Ter
|
|
|
NM_001288989.1:c.4624C>T
(PLCE1)
|
NP_001275918.1:p.Gln1542Ter
|
|
|
NM_016341.3:c.4672C>T
(PLCE1)
|
NP_057425.3:p.Gln1558Ter
|
|
|
NR_033969.1:n.910G>A
(PLCE1-AS1)
|
|
|
|
XM_006717885.2:c.4672C>T
(PLCE1)
|
XP_006717948.1:p.Gln1558Ter
|
|
|
XM_006717886.2:c.4672C>T
(PLCE1)
|
XP_006717949.1:p.Gln1558Ter
|
|
|
XM_006717888.2:c.4672C>T
(PLCE1)
|
XP_006717951.1:p.Gln1558Ter
|
|
|
XM_006717889.2:c.4624C>T
(PLCE1)
|
XP_006717952.1:p.Gln1542Ter
|
|
|
XM_006717890.1:c.3748C>T
(PLCE1)
|
XP_006717953.1:p.Gln1250Ter
|
|
|
XM_011539849.1:c.4672C>T
(PLCE1)
|
XP_011538151.1:p.Gln1558Ter
|
|
|
XM_011539850.1:c.3517C>T
(PLCE1)
|
XP_011538152.1:p.Gln1173Ter
|
|
|
XM_011539851.1:c.4672C>T
(PLCE1)
|
XP_011538153.1:p.Gln1558Ter
|
|
|
XM_011539852.1:c.4672C>T
(PLCE1)
|
XP_011538154.1:p.Gln1558Ter
|
|
|
XM_006717885.4:c.4672C>T
(PLCE1)
|
XP_006717948.1:p.Gln1558Ter
|
|
|
XM_006717888.4:c.4672C>T
(PLCE1)
|
XP_006717951.1:p.Gln1558Ter
|
|
|
XM_006717889.4:c.4624C>T
(PLCE1)
|
XP_006717952.1:p.Gln1542Ter
|
|
|
XM_006717890.3:c.3748C>T
(PLCE1)
|
XP_006717953.1:p.Gln1250Ter
|
|
|
XM_011539849.3:c.4672C>T
(PLCE1)
|
XP_011538151.1:p.Gln1558Ter
|
|
|
XM_011539850.3:c.3517C>T
(PLCE1)
|
XP_011538152.1:p.Gln1173Ter
|
|
|
XM_011539851.3:c.4672C>T
(PLCE1)
|
XP_011538153.1:p.Gln1558Ter
|
|
|
XM_011539852.3:c.4672C>T
(PLCE1)
|
XP_011538154.1:p.Gln1558Ter
|
|
|
XM_017016310.2:c.4672C>T
(PLCE1)
|
XP_016871799.1:p.Gln1558Ter
|
|
|
XM_017016311.2:c.4672C>T
(PLCE1)
|
XP_016871800.1:p.Gln1558Ter
|
|
|
XM_017016312.2:c.3700C>T
(PLCE1)
|
XP_016871801.1:p.Gln1234Ter
|
|
|
NM_001288989.2:c.4624C>T
(PLCE1)
|
NP_001275918.1:p.Gln1542Ter
|
|
|
NM_016341.4:c.4672C>T
(PLCE1)
MANE Select
|
NP_057425.3:p.Gln1558Ter
|
|
