ENST00000330342.8:c.1387T>A
MANE Select
|
ENSP00000332247.2:p.Tyr463Asn
|
|
ENST00000540368.6:n.1418T>A
|
|
|
ENST00000674794.1:c.1475T>A
|
|
|
ENST00000675260.1:n.662T>A
|
|
|
ENST00000675344.1:c.*408T>A
|
ENSP00000501953.1:n.*408T>A
|
|
ENST00000330342.7:c.1387T>A
|
ENSP00000332247.2:p.Tyr463Asn
|
|
ENST00000536426.1:n.404T>A
|
|
|
ENST00000545059.5:n.4023T>A
|
|
|
NM_012463.3:c.1387T>A
|
NP_036595.2:p.Tyr463Asn
|
|
XM_005253563.1:c.1387T>A
|
XP_005253620.1:p.Tyr463Asn
|
|
XM_006719317.2:c.874T>A
|
XP_006719380.1:p.Tyr292Asn
|
|
XM_006719318.2:c.565T>A
|
XP_006719381.1:p.Tyr189Asn
|
|
XR_429088.1:n.1550T>A
|
|
|
XM_024448910.1:c.1387T>A
|
XP_024304678.1:p.Tyr463Asn
|
|
XM_024448911.1:c.874T>A
|
XP_024304679.1:p.Tyr292Asn
|
|
XM_024448912.1:c.565T>A
|
XP_024304680.1:p.Tyr189Asn
|
|
NM_012463.4:c.1387T>A
MANE Select
|
NP_036595.2:p.Tyr463Asn
|
|