ENST00000682391.1:n.1568T>C
(CCDC78)
|
|
|
ENST00000345165.10:c.1025T>C
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Val342Ala
|
|
ENST00000293889.10:c.1025T>C
(CCDC78)
|
ENSP00000293889.6:p.Val342Ala
|
|
ENST00000345165.8:c.571T>C
(CCDC78)
|
|
|
ENST00000463539.5:n.1347T>C
(CCDC78)
|
|
|
ENST00000466708.5:n.1369T>C
(CCDC78)
|
|
|
ENST00000478979.5:n.1503T>C
(CCDC78)
|
|
|
ENST00000481804.5:n.2003T>C
(CCDC78)
|
|
|
ENST00000482152.1:n.386T>C
(CCDC78)
|
|
|
ENST00000482878.5:n.1906T>C
(CCDC78)
|
|
|
ENST00000485091.5:n.1178T>C
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38498A>G
(MSLN)
|
ENSP00000482893.1:n.-49-38498A>G
|
|
NM_001031737.2:c.1025T>C
(CCDC78)
|
NP_001026907.2:p.Val342Ala
|
|
XM_006720838.1:c.1247T>C
(CCDC78)
|
XP_006720901.1:p.Val416Ala
|
|
XM_006720843.2:c.1025T>C
(CCDC78)
|
XP_006720906.1:p.Val342Ala
|
|
XM_011522356.1:c.1472T>C
(CCDC78)
|
XP_011520658.1:p.Val491Ala
|
|
XM_011522357.1:c.1460T>C
(CCDC78)
|
XP_011520659.1:p.Val487Ala
|
|
XM_011522358.1:c.1472T>C
(CCDC78)
|
XP_011520660.1:p.Val491Ala
|
|
XM_011522359.1:c.1439T>C
(CCDC78)
|
XP_011520661.1:p.Val480Ala
|
|
XM_011522360.1:c.1427T>C
(CCDC78)
|
XP_011520662.1:p.Val476Ala
|
|
XM_011522361.1:c.1472T>C
(CCDC78)
|
XP_011520663.1:p.Val491Ala
|
|
XM_011522362.1:c.1472T>C
(CCDC78)
|
XP_011520664.1:p.Val491Ala
|
|
XM_011522363.1:c.1472T>C
(CCDC78)
|
XP_011520665.1:p.Val491Ala
|
|
XM_011522364.1:c.1472T>C
(CCDC78)
|
XP_011520666.1:p.Val491Ala
|
|
XM_011522365.1:c.1259T>C
(CCDC78)
|
XP_011520667.1:p.Val420Ala
|
|
XM_011522366.1:c.1250T>C
(CCDC78)
|
XP_011520668.1:p.Val417Ala
|
|
XM_011522367.1:c.1091T>C
(CCDC78)
|
XP_011520669.1:p.Val364Ala
|
|
XM_011522368.1:c.1079T>C
(CCDC78)
|
XP_011520670.1:p.Val360Ala
|
|
XM_011522369.1:c.1037T>C
(CCDC78)
|
XP_011520671.1:p.Val346Ala
|
|
XM_011522370.1:c.869T>C
(CCDC78)
|
XP_011520672.1:p.Val290Ala
|
|
XM_011522371.1:c.584T>C
(CCDC78)
|
XP_011520673.1:p.Val195Ala
|
|
XM_006720843.4:c.1025T>C
(CCDC78)
|
XP_006720906.1:p.Val342Ala
|
|
XM_011522358.2:c.1472T>C
(CCDC78)
|
XP_011520660.1:p.Val491Ala
|
|
XM_011522371.2:c.584T>C
(CCDC78)
|
XP_011520673.1:p.Val195Ala
|
|
XM_017022929.1:c.1472T>C
(CCDC78)
|
XP_016878418.1:p.Val491Ala
|
|
XM_017022930.1:c.572T>C
(CCDC78)
|
XP_016878419.1:p.Val191Ala
|
|
XM_024450150.1:c.302T>C
(CCDC78)
|
XP_024305918.1:p.Val101Ala
|
|
XR_001751835.1:n.1811T>C
(CCDC78)
|
|
|
XR_001751836.1:n.1790T>C
(CCDC78)
|
|
|
XR_001751837.1:n.1568T>C
(CCDC78)
|
|
|
XR_001751838.1:n.1914T>C
(CCDC78)
|
|
|
XR_001751839.1:n.1376T>C
(CCDC78)
|
|
|
NM_001031737.3:c.1025T>C
(CCDC78)
|
NP_001026907.2:p.Val342Ala
|
|
NM_001378030.1:c.1025T>C
(CCDC78)
MANE Select
|
NP_001364959.1:p.Val342Ala
|
|
NM_001378031.1:c.953+188T>C
(CCDC78)
|
NP_001364960.1:n.953+188T>C
|
|
NM_001378033.1:c.458T>C
(CCDC78)
|
NP_001364962.1:p.Val153Ala
|
|
NR_165382.1:n.1582T>C
(CCDC78)
|
|
|
NR_165383.1:n.1228T>C
(CCDC78)
|
|
|
NR_165384.1:n.1193T>C
(CCDC78)
|
|
|
NR_165385.1:n.1293T>C
(CCDC78)
|
|
|
NR_165386.1:n.1360T>C
(CCDC78)
|
|
|