ENST00000380649.8:c.1775G>T
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Gly592Val
|
|
ENST00000492433.2:c.1775G>T
(HADHA)
|
ENSP00000438039.2:p.Gly592Val
|
|
ENST00000643057.1:c.*1666G>T
(HADHA)
|
ENSP00000493761.1:n.*1666G>T
|
|
ENST00000643063.1:c.*821G>T
(HADHA)
|
ENSP00000495353.1:n.*821G>T
|
|
ENST00000643233.1:c.*1666G>T
(HADHA)
|
ENSP00000493880.1:n.*1666G>T
|
|
ENST00000644428.1:c.*399G>T
(HADHA)
|
ENSP00000495560.1:n.*399G>T
|
|
ENST00000645274.1:c.1670G>T
(HADHA)
|
ENSP00000493996.1:p.Gly557Val
|
|
ENST00000646031.1:c.1134G>T
(HADHA)
|
|
|
ENST00000646483.1:c.1641G>T
(HADHA)
|
ENSP00000496185.1:n.1641G>T
|
|
ENST00000380649.7:c.1775G>T
(HADHA)
|
ENSP00000370023.3:p.Gly592Val
|
|
ENST00000492433.1:c.233G>T
(HADHA)
|
ENSP00000438039.1:p.Gly78Val
|
|
NM_000182.4:c.1775G>T
(HADHA)
|
NP_000173.2:p.Gly592Val
|
|
XM_011532567.1:c.1683+6372C>A
(GAREM2)
|
XP_011530869.1:n.1683+6372C>A
|
|
XM_011532567.3:c.1683+6372C>A
(GAREM2)
|
XP_011530869.1:n.1683+6372C>A
|
|
NM_000182.5:c.1775G>T
(HADHA)
MANE Select
|
NP_000173.2:p.Gly592Val
|
|