ENST00000682391.1:n.1587G>T
(CCDC78)
|
|
|
ENST00000345165.10:c.1044G>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Arg348=
|
|
ENST00000293889.10:c.1044G>T
(CCDC78)
|
ENSP00000293889.6:p.Arg348=
|
|
ENST00000345165.8:c.590G>T
(CCDC78)
|
|
|
ENST00000463539.5:n.1366G>T
(CCDC78)
|
|
|
ENST00000466708.5:n.1388G>T
(CCDC78)
|
|
|
ENST00000478979.5:n.1522G>T
(CCDC78)
|
|
|
ENST00000481804.5:n.2022G>T
(CCDC78)
|
|
|
ENST00000482152.1:n.405G>T
(CCDC78)
|
|
|
ENST00000482878.5:n.1925G>T
(CCDC78)
|
|
|
ENST00000485091.5:n.1197G>T
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38517C>A
(MSLN)
|
ENSP00000482893.1:n.-49-38517C>A
|
|
NM_001031737.2:c.1044G>T
(CCDC78)
|
NP_001026907.2:p.Arg348=
|
|
XM_006720838.1:c.1266G>T
(CCDC78)
|
XP_006720901.1:p.Arg422=
|
|
XM_006720843.2:c.1044G>T
(CCDC78)
|
XP_006720906.1:p.Arg348=
|
|
XM_011522356.1:c.1491G>T
(CCDC78)
|
XP_011520658.1:p.Arg497=
|
|
XM_011522357.1:c.1479G>T
(CCDC78)
|
XP_011520659.1:p.Arg493=
|
|
XM_011522358.1:c.1491G>T
(CCDC78)
|
XP_011520660.1:p.Arg497=
|
|
XM_011522359.1:c.1458G>T
(CCDC78)
|
XP_011520661.1:p.Arg486=
|
|
XM_011522360.1:c.1446G>T
(CCDC78)
|
XP_011520662.1:p.Arg482=
|
|
XM_011522361.1:c.1491G>T
(CCDC78)
|
XP_011520663.1:p.Arg497=
|
|
XM_011522362.1:c.1491G>T
(CCDC78)
|
XP_011520664.1:p.Arg497=
|
|
XM_011522363.1:c.1491G>T
(CCDC78)
|
XP_011520665.1:p.Arg497=
|
|
XM_011522364.1:c.1491G>T
(CCDC78)
|
XP_011520666.1:p.Arg497=
|
|
XM_011522365.1:c.1278G>T
(CCDC78)
|
XP_011520667.1:p.Arg426=
|
|
XM_011522366.1:c.1269G>T
(CCDC78)
|
XP_011520668.1:p.Arg423=
|
|
XM_011522367.1:c.1110G>T
(CCDC78)
|
XP_011520669.1:p.Arg370=
|
|
XM_011522368.1:c.1098G>T
(CCDC78)
|
XP_011520670.1:p.Arg366=
|
|
XM_011522369.1:c.1056G>T
(CCDC78)
|
XP_011520671.1:p.Arg352=
|
|
XM_011522370.1:c.888G>T
(CCDC78)
|
XP_011520672.1:p.Arg296=
|
|
XM_011522371.1:c.603G>T
(CCDC78)
|
XP_011520673.1:p.Arg201=
|
|
XM_006720843.4:c.1044G>T
(CCDC78)
|
XP_006720906.1:p.Arg348=
|
|
XM_011522358.2:c.1491G>T
(CCDC78)
|
XP_011520660.1:p.Arg497=
|
|
XM_011522371.2:c.603G>T
(CCDC78)
|
XP_011520673.1:p.Arg201=
|
|
XM_017022929.1:c.1491G>T
(CCDC78)
|
XP_016878418.1:p.Arg497=
|
|
XM_017022930.1:c.591G>T
(CCDC78)
|
XP_016878419.1:p.Arg197=
|
|
XM_024450150.1:c.321G>T
(CCDC78)
|
XP_024305918.1:p.Arg107=
|
|
XR_001751835.1:n.1830G>T
(CCDC78)
|
|
|
XR_001751836.1:n.1809G>T
(CCDC78)
|
|
|
XR_001751837.1:n.1587G>T
(CCDC78)
|
|
|
XR_001751838.1:n.1933G>T
(CCDC78)
|
|
|
XR_001751839.1:n.1395G>T
(CCDC78)
|
|
|
NM_001031737.3:c.1044G>T
(CCDC78)
|
NP_001026907.2:p.Arg348=
|
|
NM_001378030.1:c.1044G>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Arg348=
|
|
NM_001378031.1:c.953+207G>T
(CCDC78)
|
NP_001364960.1:n.953+207G>T
|
|
NM_001378033.1:c.477G>T
(CCDC78)
|
NP_001364962.1:p.Arg159=
|
|
NR_165382.1:n.1601G>T
(CCDC78)
|
|
|
NR_165383.1:n.1247G>T
(CCDC78)
|
|
|
NR_165384.1:n.1212G>T
(CCDC78)
|
|
|
NR_165385.1:n.1312G>T
(CCDC78)
|
|
|
NR_165386.1:n.1379G>T
(CCDC78)
|
|
|