|
ENST00000682391.1:n.1612G>T
(CCDC78)
|
|
|
|
ENST00000345165.10:c.1069G>T
(CCDC78)
MANE Select
|
ENSP00000316851.5:p.Ala357Ser
|
|
|
ENST00000293889.10:c.1069G>T
(CCDC78)
|
ENSP00000293889.6:p.Ala357Ser
|
|
|
ENST00000345165.8:c.615G>T
(CCDC78)
|
|
|
|
ENST00000463539.5:n.1391G>T
(CCDC78)
|
|
|
|
ENST00000466708.5:n.1413G>T
(CCDC78)
|
|
|
|
ENST00000478979.5:n.1716G>T
(CCDC78)
|
|
|
|
ENST00000481804.5:n.2047G>T
(CCDC78)
|
|
|
|
ENST00000482152.1:n.430G>T
(CCDC78)
|
|
|
|
ENST00000482878.5:n.2119G>T
(CCDC78)
|
|
|
|
ENST00000485091.5:n.1222G>T
(CCDC78)
|
|
|
|
ENST00000620831.4:c.-49-38711C>A
(MSLN)
|
ENSP00000482893.1:n.-49-38711C>A
|
|
|
NM_001031737.2:c.1069G>T
(CCDC78)
|
NP_001026907.2:p.Ala357Ser
|
|
|
XM_006720838.1:c.1291G>T
(CCDC78)
|
XP_006720901.1:p.Ala431Ser
|
|
|
XM_006720843.2:c.1069G>T
(CCDC78)
|
XP_006720906.1:p.Ala357Ser
|
|
|
XM_011522356.1:c.1516G>T
(CCDC78)
|
XP_011520658.1:p.Ala506Ser
|
|
|
XM_011522357.1:c.1504G>T
(CCDC78)
|
XP_011520659.1:p.Ala502Ser
|
|
|
XM_011522358.1:c.1516G>T
(CCDC78)
|
XP_011520660.1:p.Ala506Ser
|
|
|
XM_011522359.1:c.1483G>T
(CCDC78)
|
XP_011520661.1:p.Ala495Ser
|
|
|
XM_011522360.1:c.1471G>T
(CCDC78)
|
XP_011520662.1:p.Ala491Ser
|
|
|
XM_011522361.1:c.1516G>T
(CCDC78)
|
XP_011520663.1:p.Ala506Ser
|
|
|
XM_011522362.1:c.1516G>T
(CCDC78)
|
XP_011520664.1:p.Ala506Ser
|
|
|
XM_011522363.1:c.1516G>T
(CCDC78)
|
XP_011520665.1:p.Ala506Ser
|
|
|
XM_011522364.1:c.1516G>T
(CCDC78)
|
XP_011520666.1:p.Ala506Ser
|
|
|
XM_011522365.1:c.1303G>T
(CCDC78)
|
XP_011520667.1:p.Ala435Ser
|
|
|
XM_011522366.1:c.1294G>T
(CCDC78)
|
XP_011520668.1:p.Ala432Ser
|
|
|
XM_011522367.1:c.1135G>T
(CCDC78)
|
XP_011520669.1:p.Ala379Ser
|
|
|
XM_011522368.1:c.1123G>T
(CCDC78)
|
XP_011520670.1:p.Ala375Ser
|
|
|
XM_011522369.1:c.1081G>T
(CCDC78)
|
XP_011520671.1:p.Ala361Ser
|
|
|
XM_011522370.1:c.913G>T
(CCDC78)
|
XP_011520672.1:p.Ala305Ser
|
|
|
XM_011522371.1:c.628G>T
(CCDC78)
|
XP_011520673.1:p.Ala210Ser
|
|
|
XM_006720843.4:c.1069G>T
(CCDC78)
|
XP_006720906.1:p.Ala357Ser
|
|
|
XM_011522358.2:c.1516G>T
(CCDC78)
|
XP_011520660.1:p.Ala506Ser
|
|
|
XM_011522371.2:c.628G>T
(CCDC78)
|
XP_011520673.1:p.Ala210Ser
|
|
|
XM_017022929.1:c.1516G>T
(CCDC78)
|
XP_016878418.1:p.Ala506Ser
|
|
|
XM_017022930.1:c.616G>T
(CCDC78)
|
XP_016878419.1:p.Ala206Ser
|
|
|
XM_017022931.1:c.-185G>T
(CCDC78)
|
XP_016878420.1:n.-185G>T
|
|
|
XM_024450150.1:c.346G>T
(CCDC78)
|
XP_024305918.1:p.Ala116Ser
|
|
|
XR_001751835.1:n.1855G>T
(CCDC78)
|
|
|
|
XR_001751836.1:n.1834G>T
(CCDC78)
|
|
|
|
XR_001751837.1:n.1612G>T
(CCDC78)
|
|
|
|
XR_001751838.1:n.1958G>T
(CCDC78)
|
|
|
|
XR_001751839.1:n.1420G>T
(CCDC78)
|
|
|
|
NM_001031737.3:c.1069G>T
(CCDC78)
|
NP_001026907.2:p.Ala357Ser
|
|
|
NM_001378030.1:c.1069G>T
(CCDC78)
MANE Select
|
NP_001364959.1:p.Ala357Ser
|
|
|
NM_001378031.1:c.953+401G>T
(CCDC78)
|
NP_001364960.1:n.953+401G>T
|
|
|
NM_001378033.1:c.502G>T
(CCDC78)
|
NP_001364962.1:p.Ala168Ser
|
|
|
NR_165382.1:n.1626G>T
(CCDC78)
|
|
|
|
NR_165383.1:n.1272G>T
(CCDC78)
|
|
|
|
NR_165384.1:n.1237G>T
(CCDC78)
|
|
|
|
NR_165385.1:n.1337G>T
(CCDC78)
|
|
|
|
NR_165386.1:n.1404G>T
(CCDC78)
|
|
|
