ENST00000344887.10:c.282+4C>T
MANE Select
|
ENSP00000341838.5:n.282+4C>T
|
|
ENST00000665070.1:c.282+4C>T
|
ENSP00000499482.1:n.282+4C>T
|
|
ENST00000344887.9:c.282+4C>T
|
ENSP00000341838.5:n.282+4C>T
|
|
ENST00000585806.5:n.281+4C>T
|
|
|
ENST00000586669.5:n.290+4C>T
|
|
|
ENST00000587176.5:n.466+4C>T
|
|
|
ENST00000587871.1:c.901+4C>T
|
|
|
ENST00000588882.1:c.207+4C>T
|
ENSP00000466729.1:n.207+4C>T
|
|
ENST00000590463.1:n.454+4C>T
|
|
|
NM_000363.4:c.282+4C>T , LRG_432t1:c.282+4C>T
|
NP_000354.4:n.282+4C>T
|
|
NM_000363.5:c.282+4C>T
MANE Select
|
NP_000354.4:n.282+4C>T
|
|