|
NM_006767.4:c.1665G>A
MANE Select
|
NP_006758.2:p.Leu555=
|
|
ENST00000646124.2:c.1665G>A
MANE Select
|
ENSP00000496779.1:p.Leu555=
|
|
NM_006767.3:c.1665G>A
|
NP_006758.2:p.Leu555=
|
|
ENST00000215739.12:c.1665G>A
|
ENSP00000215739.8:p.Leu555=
|
|
ENST00000415354.6:c.44-67G>A
|
ENSP00000393765.2:n.44-67G>A
|
|
ENST00000415817.2:c.22G>A
|
|
|
ENST00000479606.5:n.1811G>A
|
|
|
ENST00000491432.5:n.131G>A
|
|
|
ENST00000495142.5:n.281G>A
|
|
|
ENST00000495142.6:n.1298G>A
|
|
|
ENST00000642151.1:c.1496G>A
|
|
|
ENST00000643578.1:n.1687G>A
|
|
|
ENST00000643710.1:n.526G>A
|
|
|
ENST00000646506.1:n.1532G>A
|
|
|
ENST00000700578.1:c.1665G>A
|
ENSP00000515073.1:p.Leu555=
|