ENST00000262027.10:c.1389G=
MANE Select
|
ENSP00000262027.5:p.Glu463=
|
|
ENST00000262027.9:c.1389G=
|
ENSP00000262027.5:p.Glu463=
|
|
ENST00000447721.6:n.1031G=
|
|
|
ENST00000537638.6:c.1389G=
|
ENSP00000446168.2:p.Glu463=
|
|
ENST00000545888.6:c.*890G=
|
ENSP00000439307.2:n.*890G=
|
|
ENST00000546971.5:n.133G=
|
|
|
ENST00000548944.1:c.134-4777G=
|
ENSP00000449071.1:n.134-4777G=
|
|
ENST00000549603.1:n.335G=
|
|
|
ENST00000628866.2:c.*890G=
|
ENSP00000486738.1:n.*890G=
|
|
NM_004990.3:c.1389G=
|
NP_004981.2:p.Glu463=
|
|
XM_006719398.2:c.687G=
|
XP_006719461.1:p.Glu229=
|
|
XM_011538353.1:c.1389G=
|
XP_011536655.1:p.Glu463=
|
|
XM_006719398.4:c.687G=
|
XP_006719461.1:p.Glu229=
|
|
XR_001748704.2:n.1412G=
|
|
|
XR_002957327.1:n.1336G=
|
|
|
NM_004990.4:c.1389G=
MANE Select
|
NP_004981.2:p.Glu463=
|
|