ENST00000380649.8:c.2147G>T
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Gly716Val
|
|
ENST00000492433.2:c.2234G>T
(HADHA)
|
ENSP00000438039.2:p.Gly745Val
|
|
ENST00000643057.1:c.*2125G>T
(HADHA)
|
ENSP00000493761.1:n.*2125G>T
|
|
ENST00000643063.1:c.*1193G>T
(HADHA)
|
ENSP00000495353.1:n.*1193G>T
|
|
ENST00000643233.1:c.*2038G>T
(HADHA)
|
ENSP00000493880.1:n.*2038G>T
|
|
ENST00000644428.1:c.*771G>T
(HADHA)
|
ENSP00000495560.1:n.*771G>T
|
|
ENST00000645274.1:c.2042G>T
(HADHA)
|
ENSP00000493996.1:p.Gly681Val
|
|
ENST00000646031.1:c.1506G>T
(HADHA)
|
|
|
ENST00000646483.1:c.2013G>T
(HADHA)
|
ENSP00000496185.1:n.2013G>T
|
|
ENST00000380649.7:c.2147G>T
(HADHA)
|
ENSP00000370023.3:p.Gly716Val
|
|
ENST00000492433.1:c.692G>T
(HADHA)
|
ENSP00000438039.1:p.Gly231Val
|
|
NM_000182.4:c.2147G>T
(HADHA)
|
NP_000173.2:p.Gly716Val
|
|
XM_011532567.1:c.1683+4080C>A
(GAREM2)
|
XP_011530869.1:n.1683+4080C>A
|
|
XM_011532567.3:c.1683+4080C>A
(GAREM2)
|
XP_011530869.1:n.1683+4080C>A
|
|
NM_000182.5:c.2147G>T
(HADHA)
MANE Select
|
NP_000173.2:p.Gly716Val
|
|