ENST00000682391.1:n.1591G>T
(CCDC78)
|
|
|
ENST00000345165.10:c.1048G>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Asp350Tyr
|
|
ENST00000293889.10:c.1048G>T
(CCDC78)
|
ENSP00000293889.6:p.Asp350Tyr
|
|
ENST00000345165.8:c.594G>T
(CCDC78)
|
|
|
ENST00000463539.5:n.1370G>T
(CCDC78)
|
|
|
ENST00000466708.5:n.1392G>T
(CCDC78)
|
|
|
ENST00000478979.5:n.1526G>T
(CCDC78)
|
|
|
ENST00000481804.5:n.2026G>T
(CCDC78)
|
|
|
ENST00000482152.1:n.409G>T
(CCDC78)
|
|
|
ENST00000482878.5:n.1929G>T
(CCDC78)
|
|
|
ENST00000485091.5:n.1201G>T
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38521C>A
(MSLN)
|
ENSP00000482893.1:n.-49-38521C>A
|
|
NM_001031737.2:c.1048G>T
(CCDC78)
|
NP_001026907.2:p.Asp350Tyr
|
|
XM_006720838.1:c.1270G>T
(CCDC78)
|
XP_006720901.1:p.Asp424Tyr
|
|
XM_006720843.2:c.1048G>T
(CCDC78)
|
XP_006720906.1:p.Asp350Tyr
|
|
XM_011522356.1:c.1495G>T
(CCDC78)
|
XP_011520658.1:p.Asp499Tyr
|
|
XM_011522357.1:c.1483G>T
(CCDC78)
|
XP_011520659.1:p.Asp495Tyr
|
|
XM_011522358.1:c.1495G>T
(CCDC78)
|
XP_011520660.1:p.Asp499Tyr
|
|
XM_011522359.1:c.1462G>T
(CCDC78)
|
XP_011520661.1:p.Asp488Tyr
|
|
XM_011522360.1:c.1450G>T
(CCDC78)
|
XP_011520662.1:p.Asp484Tyr
|
|
XM_011522361.1:c.1495G>T
(CCDC78)
|
XP_011520663.1:p.Asp499Tyr
|
|
XM_011522362.1:c.1495G>T
(CCDC78)
|
XP_011520664.1:p.Asp499Tyr
|
|
XM_011522363.1:c.1495G>T
(CCDC78)
|
XP_011520665.1:p.Asp499Tyr
|
|
XM_011522364.1:c.1495G>T
(CCDC78)
|
XP_011520666.1:p.Asp499Tyr
|
|
XM_011522365.1:c.1282G>T
(CCDC78)
|
XP_011520667.1:p.Asp428Tyr
|
|
XM_011522366.1:c.1273G>T
(CCDC78)
|
XP_011520668.1:p.Asp425Tyr
|
|
XM_011522367.1:c.1114G>T
(CCDC78)
|
XP_011520669.1:p.Asp372Tyr
|
|
XM_011522368.1:c.1102G>T
(CCDC78)
|
XP_011520670.1:p.Asp368Tyr
|
|
XM_011522369.1:c.1060G>T
(CCDC78)
|
XP_011520671.1:p.Asp354Tyr
|
|
XM_011522370.1:c.892G>T
(CCDC78)
|
XP_011520672.1:p.Asp298Tyr
|
|
XM_011522371.1:c.607G>T
(CCDC78)
|
XP_011520673.1:p.Asp203Tyr
|
|
XM_006720843.4:c.1048G>T
(CCDC78)
|
XP_006720906.1:p.Asp350Tyr
|
|
XM_011522358.2:c.1495G>T
(CCDC78)
|
XP_011520660.1:p.Asp499Tyr
|
|
XM_011522371.2:c.607G>T
(CCDC78)
|
XP_011520673.1:p.Asp203Tyr
|
|
XM_017022929.1:c.1495G>T
(CCDC78)
|
XP_016878418.1:p.Asp499Tyr
|
|
XM_017022930.1:c.595G>T
(CCDC78)
|
XP_016878419.1:p.Asp199Tyr
|
|
XM_024450150.1:c.325G>T
(CCDC78)
|
XP_024305918.1:p.Asp109Tyr
|
|
XR_001751835.1:n.1834G>T
(CCDC78)
|
|
|
XR_001751836.1:n.1813G>T
(CCDC78)
|
|
|
XR_001751837.1:n.1591G>T
(CCDC78)
|
|
|
XR_001751838.1:n.1937G>T
(CCDC78)
|
|
|
XR_001751839.1:n.1399G>T
(CCDC78)
|
|
|
NM_001031737.3:c.1048G>T
(CCDC78)
|
NP_001026907.2:p.Asp350Tyr
|
|
NM_001378030.1:c.1048G>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Asp350Tyr
|
|
NM_001378031.1:c.953+211G>T
(CCDC78)
|
NP_001364960.1:n.953+211G>T
|
|
NM_001378033.1:c.481G>T
(CCDC78)
|
NP_001364962.1:p.Asp161Tyr
|
|
NR_165382.1:n.1605G>T
(CCDC78)
|
|
|
NR_165383.1:n.1251G>T
(CCDC78)
|
|
|
NR_165384.1:n.1216G>T
(CCDC78)
|
|
|
NR_165385.1:n.1316G>T
(CCDC78)
|
|
|
NR_165386.1:n.1383G>T
(CCDC78)
|
|
|