ENST00000380649.8:c.*119T>G
(HADHA)
MANE Select
|
ENSP00000370023.3:n.*119T>G
|
|
ENST00000492433.2:c.*119T>G
(HADHA)
|
ENSP00000438039.2:n.*119T>G
|
|
ENST00000643057.1:c.*2389T>G
(HADHA)
|
ENSP00000493761.1:n.*2389T>G
|
|
ENST00000643063.1:c.*1457T>G
(HADHA)
|
ENSP00000495353.1:n.*1457T>G
|
|
ENST00000643233.1:c.*2302T>G
(HADHA)
|
ENSP00000493880.1:n.*2302T>G
|
|
ENST00000644428.1:c.*1035T>G
(HADHA)
|
ENSP00000495560.1:n.*1035T>G
|
|
ENST00000645274.1:c.*119T>G
(HADHA)
|
ENSP00000493996.1:n.*119T>G
|
|
ENST00000646031.1:c.1770T>G
(HADHA)
|
|
|
ENST00000380649.7:c.*119T>G
(HADHA)
|
ENSP00000370023.3:n.*119T>G
|
|
NM_000182.4:c.*119T>G
(HADHA)
|
NP_000173.2:n.*119T>G
|
|
XM_011532567.1:c.1683+3816A>C
(GAREM2)
|
XP_011530869.1:n.1683+3816A>C
|
|
XM_011532567.3:c.1683+3816A>C
(GAREM2)
|
XP_011530869.1:n.1683+3816A>C
|
|
NM_000182.5:c.*119T>G
(HADHA)
MANE Select
|
NP_000173.2:n.*119T>G
|
|