ENST00000380649.8:c.2226A>T
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Lys742Asn
|
|
ENST00000492433.2:c.2313A>T
(HADHA)
|
ENSP00000438039.2:p.Lys771Asn
|
|
ENST00000643057.1:c.*2204A>T
(HADHA)
|
ENSP00000493761.1:n.*2204A>T
|
|
ENST00000643063.1:c.*1272A>T
(HADHA)
|
ENSP00000495353.1:n.*1272A>T
|
|
ENST00000643233.1:c.*2117A>T
(HADHA)
|
ENSP00000493880.1:n.*2117A>T
|
|
ENST00000644428.1:c.*850A>T
(HADHA)
|
ENSP00000495560.1:n.*850A>T
|
|
ENST00000645274.1:c.2121A>T
(HADHA)
|
ENSP00000493996.1:p.Lys707Asn
|
|
ENST00000646031.1:c.1585A>T
(HADHA)
|
|
|
ENST00000646483.1:c.2092A>T
(HADHA)
|
ENSP00000496185.1:n.2092A>T
|
|
ENST00000380649.7:c.2226A>T
(HADHA)
|
ENSP00000370023.3:p.Lys742Asn
|
|
NM_000182.4:c.2226A>T
(HADHA)
|
NP_000173.2:p.Lys742Asn
|
|
XM_011532567.1:c.1683+4001T>A
(GAREM2)
|
XP_011530869.1:n.1683+4001T>A
|
|
XM_011532567.3:c.1683+4001T>A
(GAREM2)
|
XP_011530869.1:n.1683+4001T>A
|
|
NM_000182.5:c.2226A>T
(HADHA)
MANE Select
|
NP_000173.2:p.Lys742Asn
|
|