ENST00000281043.4:c.141G>A
(MYCN)
MANE Select
|
ENSP00000281043.3:p.Glu47=
|
|
ENST00000638417.1:c.157+1462G>A
(MYCN)
|
ENSP00000491476.1:n.157+1462G>A
|
|
ENST00000281043.3:c.141G>A
(MYCN)
|
ENSP00000281043.3:p.Glu47=
|
|
NM_001293228.1:c.141G>A
(MYCN)
|
NP_001280157.1:p.Glu47=
|
|
NM_001293231.1:c.157+1462G>A
(MYCN)
|
NP_001280160.1:n.157+1462G>A
|
|
NM_001293233.1:c.*76G>A
(MYCN)
|
NP_001280162.1:n.*76G>A
|
|
NM_005378.5:c.141G>A
(MYCN)
|
NP_005369.2:p.Glu47=
|
|
NM_001329968.1:c.-287C>T
(MYCNOS)
|
NP_001316897.1:n.-287C>T
|
|
XM_024452528.1:c.-234+177C>T
(MYCNOS)
|
XP_024308296.1:n.-234+177C>T
|
|
NM_005378.6:c.141G>A
(MYCN)
MANE Select
|
NP_005369.2:p.Glu47=
|
|
NM_001293228.2:c.141G>A
(MYCN)
|
NP_001280157.1:p.Glu47=
|
|
NM_001293231.2:c.157+1462G>A
(MYCN)
|
NP_001280160.1:n.157+1462G>A
|
|
NM_001293233.2:c.*76G>A
(MYCN)
|
NP_001280162.1:n.*76G>A
|
|
NR_161163.1:n.229C>T
(MYCNOS)
|
|
|