ENST00000262027.10:c.1548T>C
MANE Select
|
ENSP00000262027.5:p.Tyr516=
|
|
ENST00000262027.9:c.1548T>C
|
ENSP00000262027.5:p.Tyr516=
|
|
ENST00000447721.6:n.1190T>C
|
|
|
ENST00000537638.6:c.1548T>C
|
ENSP00000446168.2:p.Tyr516=
|
|
ENST00000545888.6:c.*1049T>C
|
ENSP00000439307.2:n.*1049T>C
|
|
ENST00000546971.5:n.292T>C
|
|
|
ENST00000548630.1:n.109T>C
|
|
|
ENST00000548944.1:c.134-4479T>C
|
ENSP00000449071.1:n.134-4479T>C
|
|
ENST00000549048.1:n.81T>C
|
|
|
ENST00000628866.2:c.*1049T>C
|
ENSP00000486738.1:n.*1049T>C
|
|
NM_004990.3:c.1548T>C
|
NP_004981.2:p.Tyr516=
|
|
XM_006719398.2:c.846T>C
|
XP_006719461.1:p.Tyr282=
|
|
XM_011538353.1:c.1548T>C
|
XP_011536655.1:p.Tyr516=
|
|
XM_006719398.4:c.846T>C
|
XP_006719461.1:p.Tyr282=
|
|
XR_001748704.2:n.1571T>C
|
|
|
XR_002957327.1:n.1495T>C
|
|
|
NM_004990.4:c.1548T>C
MANE Select
|
NP_004981.2:p.Tyr516=
|
|