ENST00000380649.8:c.*7C>T
(HADHA)
MANE Select
|
ENSP00000370023.3:n.*7C>T
|
|
ENST00000492433.2:c.*7C>T
(HADHA)
|
ENSP00000438039.2:n.*7C>T
|
|
ENST00000643057.1:c.*2277C>T
(HADHA)
|
ENSP00000493761.1:n.*2277C>T
|
|
ENST00000643063.1:c.*1345C>T
(HADHA)
|
ENSP00000495353.1:n.*1345C>T
|
|
ENST00000643233.1:c.*2190C>T
(HADHA)
|
ENSP00000493880.1:n.*2190C>T
|
|
ENST00000644428.1:c.*923C>T
(HADHA)
|
ENSP00000495560.1:n.*923C>T
|
|
ENST00000645274.1:c.*7C>T
(HADHA)
|
ENSP00000493996.1:n.*7C>T
|
|
ENST00000646031.1:c.1658C>T
(HADHA)
|
|
|
ENST00000380649.7:c.*7C>T
(HADHA)
|
ENSP00000370023.3:n.*7C>T
|
|
NM_000182.4:c.*7C>T
(HADHA)
|
NP_000173.2:n.*7C>T
|
|
XM_011532567.1:c.1683+3928G>A
(GAREM2)
|
XP_011530869.1:n.1683+3928G>A
|
|
XM_011532567.3:c.1683+3928G>A
(GAREM2)
|
XP_011530869.1:n.1683+3928G>A
|
|
NM_000182.5:c.*7C>T
(HADHA)
MANE Select
|
NP_000173.2:n.*7C>T
|
|