ENST00000380649.8:c.2174G>A
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Gly725Asp
|
|
ENST00000492433.2:c.2261G>A
(HADHA)
|
ENSP00000438039.2:p.Gly754Asp
|
|
ENST00000643057.1:c.*2152G>A
(HADHA)
|
ENSP00000493761.1:n.*2152G>A
|
|
ENST00000643063.1:c.*1220G>A
(HADHA)
|
ENSP00000495353.1:n.*1220G>A
|
|
ENST00000643233.1:c.*2065G>A
(HADHA)
|
ENSP00000493880.1:n.*2065G>A
|
|
ENST00000644428.1:c.*798G>A
(HADHA)
|
ENSP00000495560.1:n.*798G>A
|
|
ENST00000645274.1:c.2069G>A
(HADHA)
|
ENSP00000493996.1:p.Gly690Asp
|
|
ENST00000646031.1:c.1533G>A
(HADHA)
|
|
|
ENST00000646483.1:c.2040G>A
(HADHA)
|
ENSP00000496185.1:n.2040G>A
|
|
ENST00000380649.7:c.2174G>A
(HADHA)
|
ENSP00000370023.3:p.Gly725Asp
|
|
ENST00000492433.1:c.719G>A
(HADHA)
|
ENSP00000438039.1:p.Gly240Asp
|
|
NM_000182.4:c.2174G>A
(HADHA)
|
NP_000173.2:p.Gly725Asp
|
|
XM_011532567.1:c.1683+4053C>T
(GAREM2)
|
XP_011530869.1:n.1683+4053C>T
|
|
XM_011532567.3:c.1683+4053C>T
(GAREM2)
|
XP_011530869.1:n.1683+4053C>T
|
|
NM_000182.5:c.2174G>A
(HADHA)
MANE Select
|
NP_000173.2:p.Gly725Asp
|
|