ENST00000380649.8:c.2073G>T
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Glu691Asp
|
|
ENST00000492433.2:c.2073G>T
(HADHA)
|
ENSP00000438039.2:p.Glu691Asp
|
|
ENST00000643057.1:c.*1964G>T
(HADHA)
|
ENSP00000493761.1:n.*1964G>T
|
|
ENST00000643063.1:c.*1119G>T
(HADHA)
|
ENSP00000495353.1:n.*1119G>T
|
|
ENST00000643233.1:c.*1964G>T
(HADHA)
|
ENSP00000493880.1:n.*1964G>T
|
|
ENST00000644428.1:c.*697G>T
(HADHA)
|
ENSP00000495560.1:n.*697G>T
|
|
ENST00000645274.1:c.1968G>T
(HADHA)
|
ENSP00000493996.1:p.Glu656Asp
|
|
ENST00000646031.1:c.1432G>T
(HADHA)
|
|
|
ENST00000646483.1:c.1939G>T
(HADHA)
|
ENSP00000496185.1:n.1939G>T
|
|
ENST00000380649.7:c.2073G>T
(HADHA)
|
ENSP00000370023.3:p.Glu691Asp
|
|
ENST00000492433.1:c.531G>T
(HADHA)
|
ENSP00000438039.1:p.Glu177Asp
|
|
NM_000182.4:c.2073G>T
(HADHA)
|
NP_000173.2:p.Glu691Asp
|
|
XM_011532567.1:c.1683+4241C>A
(GAREM2)
|
XP_011530869.1:n.1683+4241C>A
|
|
XM_011532567.3:c.1683+4241C>A
(GAREM2)
|
XP_011530869.1:n.1683+4241C>A
|
|
NM_000182.5:c.2073G>T
(HADHA)
MANE Select
|
NP_000173.2:p.Glu691Asp
|
|