ENST00000328300.11:c.4909G>A
MANE Select
|
ENSP00000331902.7:p.Glu1637Lys
|
|
ENST00000361603.7:c.4891G>A
|
ENSP00000354505.2:p.Glu1631Lys
|
|
ENST00000510690.2:n.1403G>A
|
|
|
ENST00000644079.1:n.1740G>A
|
|
|
ENST00000328300.10:c.4909G>A
|
ENSP00000331902.6:p.Glu1637Lys
|
|
ENST00000361603.6:c.4891G>A
|
ENSP00000354505.2:p.Glu1631Lys
|
|
ENST00000504541.1:c.219+433G>A
|
ENSP00000424845.1:n.219+433G>A
|
|
ENST00000515658.1:c.325-943G>A
|
|
|
NM_000495.4:c.4891G>A
|
NP_000486.1:p.Glu1631Lys
|
|
NM_033380.2:c.4909G>A
|
NP_203699.1:p.Glu1637Lys
|
|
XM_005262070.2:c.4900G>A
|
XP_005262127.1:p.Glu1634Lys
|
|
XM_006724616.2:c.4909G>A
|
XP_006724679.1:p.Glu1637Lys
|
|
XM_011530849.1:c.4585G>A
|
XP_011529151.1:p.Glu1529Lys
|
|
XM_011530851.1:c.2482G>A
|
XP_011529153.1:p.Glu828Lys
|
|
XM_011530849.2:c.4924G>A
|
XP_011529151.2:p.Glu1642Lys
|
|
XM_017029259.2:c.4915G>A
|
XP_016884748.1:p.Glu1639Lys
|
|
XM_017029260.1:c.4906G>A
|
XP_016884749.1:p.Glu1636Lys
|
|
XM_017029263.2:c.3244G>A
|
XP_016884752.1:p.Glu1082Lys
|
|
NM_000495.5:c.4891G>A
|
NP_000486.1:p.Glu1631Lys
|
|
NM_033380.3:c.4909G>A
MANE Select
|
NP_203699.1:p.Glu1637Lys
|
|