ENST00000380649.8:c.1593G>T
(HADHA)
MANE Select
|
ENSP00000370023.3:p.Lys531Asn
|
|
ENST00000492433.2:c.1593G>T
(HADHA)
|
ENSP00000438039.2:p.Lys531Asn
|
|
ENST00000643057.1:c.*1484G>T
(HADHA)
|
ENSP00000493761.1:n.*1484G>T
|
|
ENST00000643063.1:c.*639G>T
(HADHA)
|
ENSP00000495353.1:n.*639G>T
|
|
ENST00000643233.1:c.*1484G>T
(HADHA)
|
ENSP00000493880.1:n.*1484G>T
|
|
ENST00000644428.1:c.*217G>T
(HADHA)
|
ENSP00000495560.1:n.*217G>T
|
|
ENST00000645274.1:c.1488G>T
(HADHA)
|
ENSP00000493996.1:p.Lys496Asn
|
|
ENST00000646031.1:c.952G>T
(HADHA)
|
|
|
ENST00000646483.1:c.1459G>T
(HADHA)
|
ENSP00000496185.1:n.1459G>T
|
|
ENST00000380649.7:c.1593G>T
(HADHA)
|
ENSP00000370023.3:p.Lys531Asn
|
|
ENST00000492433.1:c.51G>T
(HADHA)
|
ENSP00000438039.1:p.Lys17Asn
|
|
NM_000182.4:c.1593G>T
(HADHA)
|
NP_000173.2:p.Lys531Asn
|
|
XM_011532567.1:c.1684-7114C>A
(GAREM2)
|
XP_011530869.1:n.1684-7114C>A
|
|
XM_011532567.3:c.1684-7114C>A
(GAREM2)
|
XP_011530869.1:n.1684-7114C>A
|
|
NM_000182.5:c.1593G>T
(HADHA)
MANE Select
|
NP_000173.2:p.Lys531Asn
|
|