ENST00000682391.1:n.1566G>T
(CCDC78)
|
|
|
ENST00000345165.10:c.1023G>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Leu341=
|
|
ENST00000293889.10:c.1023G>T
(CCDC78)
|
ENSP00000293889.6:p.Leu341=
|
|
ENST00000345165.8:c.569G>T
(CCDC78)
|
|
|
ENST00000463539.5:n.1345G>T
(CCDC78)
|
|
|
ENST00000466708.5:n.1367G>T
(CCDC78)
|
|
|
ENST00000478979.5:n.1501G>T
(CCDC78)
|
|
|
ENST00000481804.5:n.2001G>T
(CCDC78)
|
|
|
ENST00000482152.1:n.384G>T
(CCDC78)
|
|
|
ENST00000482878.5:n.1904G>T
(CCDC78)
|
|
|
ENST00000485091.5:n.1176G>T
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38496C>A
(MSLN)
|
ENSP00000482893.1:n.-49-38496C>A
|
|
NM_001031737.2:c.1023G>T
(CCDC78)
|
NP_001026907.2:p.Leu341=
|
|
XM_006720838.1:c.1245G>T
(CCDC78)
|
XP_006720901.1:p.Leu415=
|
|
XM_006720843.2:c.1023G>T
(CCDC78)
|
XP_006720906.1:p.Leu341=
|
|
XM_011522356.1:c.1470G>T
(CCDC78)
|
XP_011520658.1:p.Leu490=
|
|
XM_011522357.1:c.1458G>T
(CCDC78)
|
XP_011520659.1:p.Leu486=
|
|
XM_011522358.1:c.1470G>T
(CCDC78)
|
XP_011520660.1:p.Leu490=
|
|
XM_011522359.1:c.1437G>T
(CCDC78)
|
XP_011520661.1:p.Leu479=
|
|
XM_011522360.1:c.1425G>T
(CCDC78)
|
XP_011520662.1:p.Leu475=
|
|
XM_011522361.1:c.1470G>T
(CCDC78)
|
XP_011520663.1:p.Leu490=
|
|
XM_011522362.1:c.1470G>T
(CCDC78)
|
XP_011520664.1:p.Leu490=
|
|
XM_011522363.1:c.1470G>T
(CCDC78)
|
XP_011520665.1:p.Leu490=
|
|
XM_011522364.1:c.1470G>T
(CCDC78)
|
XP_011520666.1:p.Leu490=
|
|
XM_011522365.1:c.1257G>T
(CCDC78)
|
XP_011520667.1:p.Leu419=
|
|
XM_011522366.1:c.1248G>T
(CCDC78)
|
XP_011520668.1:p.Leu416=
|
|
XM_011522367.1:c.1089G>T
(CCDC78)
|
XP_011520669.1:p.Leu363=
|
|
XM_011522368.1:c.1077G>T
(CCDC78)
|
XP_011520670.1:p.Leu359=
|
|
XM_011522369.1:c.1035G>T
(CCDC78)
|
XP_011520671.1:p.Leu345=
|
|
XM_011522370.1:c.867G>T
(CCDC78)
|
XP_011520672.1:p.Leu289=
|
|
XM_011522371.1:c.582G>T
(CCDC78)
|
XP_011520673.1:p.Leu194=
|
|
XM_006720843.4:c.1023G>T
(CCDC78)
|
XP_006720906.1:p.Leu341=
|
|
XM_011522358.2:c.1470G>T
(CCDC78)
|
XP_011520660.1:p.Leu490=
|
|
XM_011522371.2:c.582G>T
(CCDC78)
|
XP_011520673.1:p.Leu194=
|
|
XM_017022929.1:c.1470G>T
(CCDC78)
|
XP_016878418.1:p.Leu490=
|
|
XM_017022930.1:c.570G>T
(CCDC78)
|
XP_016878419.1:p.Leu190=
|
|
XM_024450150.1:c.300G>T
(CCDC78)
|
XP_024305918.1:p.Leu100=
|
|
XR_001751835.1:n.1809G>T
(CCDC78)
|
|
|
XR_001751836.1:n.1788G>T
(CCDC78)
|
|
|
XR_001751837.1:n.1566G>T
(CCDC78)
|
|
|
XR_001751838.1:n.1912G>T
(CCDC78)
|
|
|
XR_001751839.1:n.1374G>T
(CCDC78)
|
|
|
NM_001031737.3:c.1023G>T
(CCDC78)
|
NP_001026907.2:p.Leu341=
|
|
NM_001378030.1:c.1023G>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Leu341=
|
|
NM_001378031.1:c.953+186G>T
(CCDC78)
|
NP_001364960.1:n.953+186G>T
|
|
NM_001378033.1:c.456G>T
(CCDC78)
|
NP_001364962.1:p.Leu152=
|
|
NR_165382.1:n.1580G>T
(CCDC78)
|
|
|
NR_165383.1:n.1226G>T
(CCDC78)
|
|
|
NR_165384.1:n.1191G>T
(CCDC78)
|
|
|
NR_165385.1:n.1291G>T
(CCDC78)
|
|
|
NR_165386.1:n.1358G>T
(CCDC78)
|
|
|