ENST00000682391.1:n.1604G>T
(CCDC78)
|
|
|
ENST00000345165.10:c.1061G>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Gly354Val
|
|
ENST00000293889.10:c.1061G>T
(CCDC78)
|
ENSP00000293889.6:p.Gly354Val
|
|
ENST00000345165.8:c.607G>T
(CCDC78)
|
|
|
ENST00000463539.5:n.1383G>T
(CCDC78)
|
|
|
ENST00000466708.5:n.1405G>T
(CCDC78)
|
|
|
ENST00000478979.5:n.1708G>T
(CCDC78)
|
|
|
ENST00000481804.5:n.2039G>T
(CCDC78)
|
|
|
ENST00000482152.1:n.422G>T
(CCDC78)
|
|
|
ENST00000482878.5:n.2111G>T
(CCDC78)
|
|
|
ENST00000485091.5:n.1214G>T
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38703C>A
(MSLN)
|
ENSP00000482893.1:n.-49-38703C>A
|
|
NM_001031737.2:c.1061G>T
(CCDC78)
|
NP_001026907.2:p.Gly354Val
|
|
XM_006720838.1:c.1283G>T
(CCDC78)
|
XP_006720901.1:p.Gly428Val
|
|
XM_006720843.2:c.1061G>T
(CCDC78)
|
XP_006720906.1:p.Gly354Val
|
|
XM_011522356.1:c.1508G>T
(CCDC78)
|
XP_011520658.1:p.Gly503Val
|
|
XM_011522357.1:c.1496G>T
(CCDC78)
|
XP_011520659.1:p.Gly499Val
|
|
XM_011522358.1:c.1508G>T
(CCDC78)
|
XP_011520660.1:p.Gly503Val
|
|
XM_011522359.1:c.1475G>T
(CCDC78)
|
XP_011520661.1:p.Gly492Val
|
|
XM_011522360.1:c.1463G>T
(CCDC78)
|
XP_011520662.1:p.Gly488Val
|
|
XM_011522361.1:c.1508G>T
(CCDC78)
|
XP_011520663.1:p.Gly503Val
|
|
XM_011522362.1:c.1508G>T
(CCDC78)
|
XP_011520664.1:p.Gly503Val
|
|
XM_011522363.1:c.1508G>T
(CCDC78)
|
XP_011520665.1:p.Gly503Val
|
|
XM_011522364.1:c.1508G>T
(CCDC78)
|
XP_011520666.1:p.Gly503Val
|
|
XM_011522365.1:c.1295G>T
(CCDC78)
|
XP_011520667.1:p.Gly432Val
|
|
XM_011522366.1:c.1286G>T
(CCDC78)
|
XP_011520668.1:p.Gly429Val
|
|
XM_011522367.1:c.1127G>T
(CCDC78)
|
XP_011520669.1:p.Gly376Val
|
|
XM_011522368.1:c.1115G>T
(CCDC78)
|
XP_011520670.1:p.Gly372Val
|
|
XM_011522369.1:c.1073G>T
(CCDC78)
|
XP_011520671.1:p.Gly358Val
|
|
XM_011522370.1:c.905G>T
(CCDC78)
|
XP_011520672.1:p.Gly302Val
|
|
XM_011522371.1:c.620G>T
(CCDC78)
|
XP_011520673.1:p.Gly207Val
|
|
XM_006720843.4:c.1061G>T
(CCDC78)
|
XP_006720906.1:p.Gly354Val
|
|
XM_011522358.2:c.1508G>T
(CCDC78)
|
XP_011520660.1:p.Gly503Val
|
|
XM_011522371.2:c.620G>T
(CCDC78)
|
XP_011520673.1:p.Gly207Val
|
|
XM_017022929.1:c.1508G>T
(CCDC78)
|
XP_016878418.1:p.Gly503Val
|
|
XM_017022930.1:c.608G>T
(CCDC78)
|
XP_016878419.1:p.Gly203Val
|
|
XM_017022931.1:c.-193G>T
(CCDC78)
|
XP_016878420.1:n.-193G>T
|
|
XM_024450150.1:c.338G>T
(CCDC78)
|
XP_024305918.1:p.Gly113Val
|
|
XR_001751835.1:n.1847G>T
(CCDC78)
|
|
|
XR_001751836.1:n.1826G>T
(CCDC78)
|
|
|
XR_001751837.1:n.1604G>T
(CCDC78)
|
|
|
XR_001751838.1:n.1950G>T
(CCDC78)
|
|
|
XR_001751839.1:n.1412G>T
(CCDC78)
|
|
|
NM_001031737.3:c.1061G>T
(CCDC78)
|
NP_001026907.2:p.Gly354Val
|
|
NM_001378030.1:c.1061G>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Gly354Val
|
|
NM_001378031.1:c.953+393G>T
(CCDC78)
|
NP_001364960.1:n.953+393G>T
|
|
NM_001378033.1:c.494G>T
(CCDC78)
|
NP_001364962.1:p.Gly165Val
|
|
NR_165382.1:n.1618G>T
(CCDC78)
|
|
|
NR_165383.1:n.1264G>T
(CCDC78)
|
|
|
NR_165384.1:n.1229G>T
(CCDC78)
|
|
|
NR_165385.1:n.1329G>T
(CCDC78)
|
|
|
NR_165386.1:n.1396G>T
(CCDC78)
|
|
|