ENST00000682391.1:n.1559T>C
(CCDC78)
|
|
|
ENST00000345165.10:c.1016T>C
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Val339Ala
|
|
ENST00000293889.10:c.1016T>C
(CCDC78)
|
ENSP00000293889.6:p.Val339Ala
|
|
ENST00000345165.8:c.562T>C
(CCDC78)
|
|
|
ENST00000463539.5:n.1338T>C
(CCDC78)
|
|
|
ENST00000466708.5:n.1360T>C
(CCDC78)
|
|
|
ENST00000478979.5:n.1494T>C
(CCDC78)
|
|
|
ENST00000481804.5:n.1994T>C
(CCDC78)
|
|
|
ENST00000482152.1:n.377T>C
(CCDC78)
|
|
|
ENST00000482878.5:n.1897T>C
(CCDC78)
|
|
|
ENST00000485091.5:n.1169T>C
(CCDC78)
|
|
|
ENST00000620831.4:c.-49-38489A>G
(MSLN)
|
ENSP00000482893.1:n.-49-38489A>G
|
|
NM_001031737.2:c.1016T>C
(CCDC78)
|
NP_001026907.2:p.Val339Ala
|
|
XM_006720838.1:c.1238T>C
(CCDC78)
|
XP_006720901.1:p.Val413Ala
|
|
XM_006720843.2:c.1016T>C
(CCDC78)
|
XP_006720906.1:p.Val339Ala
|
|
XM_011522356.1:c.1463T>C
(CCDC78)
|
XP_011520658.1:p.Val488Ala
|
|
XM_011522357.1:c.1451T>C
(CCDC78)
|
XP_011520659.1:p.Val484Ala
|
|
XM_011522358.1:c.1463T>C
(CCDC78)
|
XP_011520660.1:p.Val488Ala
|
|
XM_011522359.1:c.1430T>C
(CCDC78)
|
XP_011520661.1:p.Val477Ala
|
|
XM_011522360.1:c.1418T>C
(CCDC78)
|
XP_011520662.1:p.Val473Ala
|
|
XM_011522361.1:c.1463T>C
(CCDC78)
|
XP_011520663.1:p.Val488Ala
|
|
XM_011522362.1:c.1463T>C
(CCDC78)
|
XP_011520664.1:p.Val488Ala
|
|
XM_011522363.1:c.1463T>C
(CCDC78)
|
XP_011520665.1:p.Val488Ala
|
|
XM_011522364.1:c.1463T>C
(CCDC78)
|
XP_011520666.1:p.Val488Ala
|
|
XM_011522365.1:c.1250T>C
(CCDC78)
|
XP_011520667.1:p.Val417Ala
|
|
XM_011522366.1:c.1241T>C
(CCDC78)
|
XP_011520668.1:p.Val414Ala
|
|
XM_011522367.1:c.1082T>C
(CCDC78)
|
XP_011520669.1:p.Val361Ala
|
|
XM_011522368.1:c.1070T>C
(CCDC78)
|
XP_011520670.1:p.Val357Ala
|
|
XM_011522369.1:c.1028T>C
(CCDC78)
|
XP_011520671.1:p.Val343Ala
|
|
XM_011522370.1:c.860T>C
(CCDC78)
|
XP_011520672.1:p.Val287Ala
|
|
XM_011522371.1:c.575T>C
(CCDC78)
|
XP_011520673.1:p.Val192Ala
|
|
XM_006720843.4:c.1016T>C
(CCDC78)
|
XP_006720906.1:p.Val339Ala
|
|
XM_011522358.2:c.1463T>C
(CCDC78)
|
XP_011520660.1:p.Val488Ala
|
|
XM_011522371.2:c.575T>C
(CCDC78)
|
XP_011520673.1:p.Val192Ala
|
|
XM_017022929.1:c.1463T>C
(CCDC78)
|
XP_016878418.1:p.Val488Ala
|
|
XM_017022930.1:c.563T>C
(CCDC78)
|
XP_016878419.1:p.Val188Ala
|
|
XM_024450150.1:c.293T>C
(CCDC78)
|
XP_024305918.1:p.Val98Ala
|
|
XR_001751835.1:n.1802T>C
(CCDC78)
|
|
|
XR_001751836.1:n.1781T>C
(CCDC78)
|
|
|
XR_001751837.1:n.1559T>C
(CCDC78)
|
|
|
XR_001751838.1:n.1905T>C
(CCDC78)
|
|
|
XR_001751839.1:n.1367T>C
(CCDC78)
|
|
|
NM_001031737.3:c.1016T>C
(CCDC78)
|
NP_001026907.2:p.Val339Ala
|
|
NM_001378030.1:c.1016T>C
(CCDC78)
MANE Select
|
NP_001364959.1:p.Val339Ala
|
|
NM_001378031.1:c.953+179T>C
(CCDC78)
|
NP_001364960.1:n.953+179T>C
|
|
NM_001378033.1:c.449T>C
(CCDC78)
|
NP_001364962.1:p.Val150Ala
|
|
NR_165382.1:n.1573T>C
(CCDC78)
|
|
|
NR_165383.1:n.1219T>C
(CCDC78)
|
|
|
NR_165384.1:n.1184T>C
(CCDC78)
|
|
|
NR_165385.1:n.1284T>C
(CCDC78)
|
|
|
NR_165386.1:n.1351T>C
(CCDC78)
|
|
|