ENST00000262027.10:c.1596C>A
MANE Select
|
ENSP00000262027.5:p.Tyr532Ter
|
|
ENST00000262027.9:c.1596C>A
|
ENSP00000262027.5:p.Tyr532Ter
|
|
ENST00000447721.6:n.1238C>A
|
|
|
ENST00000537638.6:c.1596C>A
|
ENSP00000446168.2:p.Tyr532Ter
|
|
ENST00000545888.6:c.*1097C>A
|
ENSP00000439307.2:n.*1097C>A
|
|
ENST00000546971.5:n.340C>A
|
|
|
ENST00000548630.1:n.157C>A
|
|
|
ENST00000548944.1:c.134-4431C>A
|
ENSP00000449071.1:n.134-4431C>A
|
|
ENST00000549048.1:n.129C>A
|
|
|
ENST00000628866.2:c.*1097C>A
|
ENSP00000486738.1:n.*1097C>A
|
|
NM_004990.3:c.1596C>A
|
NP_004981.2:p.Tyr532Ter
|
|
XM_006719398.2:c.894C>A
|
XP_006719461.1:p.Tyr298Ter
|
|
XM_011538353.1:c.1596C>A
|
XP_011536655.1:p.Tyr532Ter
|
|
XM_006719398.4:c.894C>A
|
XP_006719461.1:p.Tyr298Ter
|
|
XR_001748704.2:n.1619C>A
|
|
|
XR_002957327.1:n.1543C>A
|
|
|
NM_004990.4:c.1596C>A
MANE Select
|
NP_004981.2:p.Tyr532Ter
|
|