ENST00000328300.11:c.4942G>A
MANE Select
|
ENSP00000331902.7:p.Ala1648Thr
|
|
ENST00000361603.7:c.4924G>A
|
ENSP00000354505.2:p.Ala1642Thr
|
|
ENST00000510690.2:n.1436G>A
|
|
|
ENST00000644079.1:n.1773G>A
|
|
|
ENST00000328300.10:c.4942G>A
|
ENSP00000331902.6:p.Ala1648Thr
|
|
ENST00000361603.6:c.4924G>A
|
ENSP00000354505.2:p.Ala1642Thr
|
|
ENST00000504541.1:c.219+466G>A
|
ENSP00000424845.1:n.219+466G>A
|
|
ENST00000515658.1:c.325-910G>A
|
|
|
NM_000495.4:c.4924G>A
|
NP_000486.1:p.Ala1642Thr
|
|
NM_033380.2:c.4942G>A
|
NP_203699.1:p.Ala1648Thr
|
|
XM_005262070.2:c.4933G>A
|
XP_005262127.1:p.Ala1645Thr
|
|
XM_006724616.2:c.4942G>A
|
XP_006724679.1:p.Ala1648Thr
|
|
XM_011530849.1:c.4618G>A
|
XP_011529151.1:p.Ala1540Thr
|
|
XM_011530851.1:c.2515G>A
|
XP_011529153.1:p.Ala839Thr
|
|
XM_011530849.2:c.4957G>A
|
XP_011529151.2:p.Ala1653Thr
|
|
XM_017029259.2:c.4948G>A
|
XP_016884748.1:p.Ala1650Thr
|
|
XM_017029260.1:c.4939G>A
|
XP_016884749.1:p.Ala1647Thr
|
|
XM_017029263.2:c.3277G>A
|
XP_016884752.1:p.Ala1093Thr
|
|
NM_000495.5:c.4924G>A
|
NP_000486.1:p.Ala1642Thr
|
|
NM_033380.3:c.4942G>A
MANE Select
|
NP_203699.1:p.Ala1648Thr
|
|