|
ENST00000682391.1:n.1650C>T
(CCDC78)
|
|
|
|
ENST00000345165.10:c.1107C>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Ala369=
|
|
|
ENST00000293889.10:c.1107C>T
(CCDC78)
|
ENSP00000293889.6:p.Ala369=
|
|
|
ENST00000345165.8:c.653C>T
(CCDC78)
|
|
|
|
ENST00000463539.5:n.1429C>T
(CCDC78)
|
|
|
|
ENST00000466708.5:n.1451C>T
(CCDC78)
|
|
|
|
ENST00000478979.5:n.1754C>T
(CCDC78)
|
|
|
|
ENST00000481804.5:n.2085C>T
(CCDC78)
|
|
|
|
ENST00000482152.1:n.468C>T
(CCDC78)
|
|
|
|
ENST00000482878.5:n.2157C>T
(CCDC78)
|
|
|
|
ENST00000485091.5:n.1260C>T
(CCDC78)
|
|
|
|
ENST00000620831.4:c.-49-38749G>A
(MSLN)
|
ENSP00000482893.1:n.-49-38749G>A
|
|
|
NM_001031737.2:c.1107C>T
(CCDC78)
|
NP_001026907.2:p.Ala369=
|
|
|
XM_006720838.1:c.1329C>T
(CCDC78)
|
XP_006720901.1:p.Ala443=
|
|
|
XM_006720843.2:c.1107C>T
(CCDC78)
|
XP_006720906.1:p.Ala369=
|
|
|
XM_011522356.1:c.1554C>T
(CCDC78)
|
XP_011520658.1:p.Ala518=
|
|
|
XM_011522357.1:c.1542C>T
(CCDC78)
|
XP_011520659.1:p.Ala514=
|
|
|
XM_011522358.1:c.1554C>T
(CCDC78)
|
XP_011520660.1:p.Ala518=
|
|
|
XM_011522359.1:c.1521C>T
(CCDC78)
|
XP_011520661.1:p.Ala507=
|
|
|
XM_011522360.1:c.1509C>T
(CCDC78)
|
XP_011520662.1:p.Ala503=
|
|
|
XM_011522361.1:c.1554C>T
(CCDC78)
|
XP_011520663.1:p.Ala518=
|
|
|
XM_011522362.1:c.1554C>T
(CCDC78)
|
XP_011520664.1:p.Ala518=
|
|
|
XM_011522363.1:c.1554C>T
(CCDC78)
|
XP_011520665.1:p.Ala518=
|
|
|
XM_011522364.1:c.1554C>T
(CCDC78)
|
XP_011520666.1:p.Ala518=
|
|
|
XM_011522365.1:c.1341C>T
(CCDC78)
|
XP_011520667.1:p.Ala447=
|
|
|
XM_011522366.1:c.1332C>T
(CCDC78)
|
XP_011520668.1:p.Ala444=
|
|
|
XM_011522367.1:c.1173C>T
(CCDC78)
|
XP_011520669.1:p.Ala391=
|
|
|
XM_011522368.1:c.1161C>T
(CCDC78)
|
XP_011520670.1:p.Ala387=
|
|
|
XM_011522369.1:c.1119C>T
(CCDC78)
|
XP_011520671.1:p.Ala373=
|
|
|
XM_011522370.1:c.951C>T
(CCDC78)
|
XP_011520672.1:p.Ala317=
|
|
|
XM_011522371.1:c.666C>T
(CCDC78)
|
XP_011520673.1:p.Ala222=
|
|
|
XM_006720843.4:c.1107C>T
(CCDC78)
|
XP_006720906.1:p.Ala369=
|
|
|
XM_011522358.2:c.1554C>T
(CCDC78)
|
XP_011520660.1:p.Ala518=
|
|
|
XM_011522371.2:c.666C>T
(CCDC78)
|
XP_011520673.1:p.Ala222=
|
|
|
XM_017022929.1:c.1554C>T
(CCDC78)
|
XP_016878418.1:p.Ala518=
|
|
|
XM_017022930.1:c.654C>T
(CCDC78)
|
XP_016878419.1:p.Ala218=
|
|
|
XM_017022931.1:c.-147C>T
(CCDC78)
|
XP_016878420.1:n.-147C>T
|
|
|
XM_024450150.1:c.384C>T
(CCDC78)
|
XP_024305918.1:p.Ala128=
|
|
|
XR_001751835.1:n.1893C>T
(CCDC78)
|
|
|
|
XR_001751836.1:n.1872C>T
(CCDC78)
|
|
|
|
XR_001751837.1:n.1650C>T
(CCDC78)
|
|
|
|
XR_001751838.1:n.1996C>T
(CCDC78)
|
|
|
|
XR_001751839.1:n.1458C>T
(CCDC78)
|
|
|
|
NM_001031737.3:c.1107C>T
(CCDC78)
|
NP_001026907.2:p.Ala369=
|
|
|
NM_001378030.1:c.1107C>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Ala369=
|
|
|
NM_001378031.1:c.953+439C>T
(CCDC78)
|
NP_001364960.1:n.953+439C>T
|
|
|
NM_001378033.1:c.540C>T
(CCDC78)
|
NP_001364962.1:p.Ala180=
|
|
|
NR_165382.1:n.1664C>T
(CCDC78)
|
|
|
|
NR_165383.1:n.1310C>T
(CCDC78)
|
|
|
|
NR_165384.1:n.1275C>T
(CCDC78)
|
|
|
|
NR_165385.1:n.1375C>T
(CCDC78)
|
|
|
|
NR_165386.1:n.1442C>T
(CCDC78)
|
|
|
