ENST00000380649.8:c.*110G>T
(HADHA)
MANE Select
|
ENSP00000370023.3:n.*110G>T
|
|
ENST00000492433.2:c.*110G>T
(HADHA)
|
ENSP00000438039.2:n.*110G>T
|
|
ENST00000643057.1:c.*2380G>T
(HADHA)
|
ENSP00000493761.1:n.*2380G>T
|
|
ENST00000643063.1:c.*1448G>T
(HADHA)
|
ENSP00000495353.1:n.*1448G>T
|
|
ENST00000643233.1:c.*2293G>T
(HADHA)
|
ENSP00000493880.1:n.*2293G>T
|
|
ENST00000644428.1:c.*1026G>T
(HADHA)
|
ENSP00000495560.1:n.*1026G>T
|
|
ENST00000645274.1:c.*110G>T
(HADHA)
|
ENSP00000493996.1:n.*110G>T
|
|
ENST00000646031.1:c.1761G>T
(HADHA)
|
|
|
ENST00000380649.7:c.*110G>T
(HADHA)
|
ENSP00000370023.3:n.*110G>T
|
|
NM_000182.4:c.*110G>T
(HADHA)
|
NP_000173.2:n.*110G>T
|
|
XM_011532567.1:c.1683+3825C>A
(GAREM2)
|
XP_011530869.1:n.1683+3825C>A
|
|
XM_011532567.3:c.1683+3825C>A
(GAREM2)
|
XP_011530869.1:n.1683+3825C>A
|
|
NM_000182.5:c.*110G>T
(HADHA)
MANE Select
|
NP_000173.2:n.*110G>T
|
|