ENST00000426263.10:c.274C=
MANE Select
|
ENSP00000416293.2:p.Arg92=
|
|
ENST00000674765.1:c.274C=
|
ENSP00000501811.1:p.Arg92=
|
|
ENST00000675112.1:n.297C=
|
|
|
ENST00000676254.1:n.723C=
|
|
|
ENST00000372500.4:c.178C=
|
ENSP00000361578.4:p.Arg60=
|
|
ENST00000415851.6:n.491C=
|
|
|
ENST00000426263.7:c.274C=
|
ENSP00000416293.2:p.Arg92=
|
|
ENST00000439722.2:c.79C=
|
ENSP00000395521.2:p.Arg27=
|
|
ENST00000475162.3:c.173C=
|
|
|
ENST00000625233.2:n.482C=
|
|
|
ENST00000630287.2:c.274C=
|
ENSP00000486694.1:p.Arg92=
|
|
NM_006516.2:c.274C=
|
NP_006507.2:p.Arg92=
|
|
NM_006516.3:c.274C=
|
NP_006507.2:p.Arg92=
|
|
NM_006516.4:c.274C=
MANE Select
|
NP_006507.2:p.Arg92=
|
|