|
NM_006767.4:c.1676T>A
MANE Select
|
NP_006758.2:p.Leu559Ter
|
|
ENST00000646124.2:c.1676T>A
MANE Select
|
ENSP00000496779.1:p.Leu559Ter
|
|
NM_006767.3:c.1676T>A
|
NP_006758.2:p.Leu559Ter
|
|
ENST00000215739.12:c.1676T>A
|
ENSP00000215739.8:p.Leu559Ter
|
|
ENST00000415354.6:c.44-56T>A
|
ENSP00000393765.2:n.44-56T>A
|
|
ENST00000415817.2:c.33T>A
|
|
|
ENST00000479606.5:n.1822T>A
|
|
|
ENST00000491432.5:n.142T>A
|
|
|
ENST00000495142.5:n.292T>A
|
|
|
ENST00000495142.6:n.1309T>A
|
|
|
ENST00000642151.1:c.1507T>A
|
|
|
ENST00000643578.1:n.1698T>A
|
|
|
ENST00000643710.1:n.537T>A
|
|
|
ENST00000646506.1:n.1543T>A
|
|
|
ENST00000700578.1:c.1676T>A
|
ENSP00000515073.1:p.Leu559Ter
|