ENST00000328300.11:c.5073A>G
MANE Select
|
ENSP00000331902.7:p.Thr1691=
|
|
ENST00000361603.7:c.5055A>G
|
ENSP00000354505.2:p.Thr1685=
|
|
ENST00000510690.2:n.1567A>G
|
|
|
ENST00000644079.1:n.2761A>G
|
|
|
ENST00000328300.10:c.5073A>G
|
ENSP00000331902.6:p.Thr1691=
|
|
ENST00000361603.6:c.5055A>G
|
ENSP00000354505.2:p.Thr1685=
|
|
ENST00000504541.1:c.298A>G
|
ENSP00000424845.1:n.298A>G
|
|
ENST00000515658.1:c.403A>G
|
|
|
NM_000495.4:c.5055A>G
|
NP_000486.1:p.Thr1685=
|
|
NM_033380.2:c.5073A>G
|
NP_203699.1:p.Thr1691=
|
|
XM_005262070.2:c.5064A>G
|
XP_005262127.1:p.Thr1688=
|
|
XM_006724616.2:c.5073A>G
|
XP_006724679.1:p.Thr1691=
|
|
XM_011530849.1:c.4749A>G
|
XP_011529151.1:p.Thr1583=
|
|
XM_011530851.1:c.2646A>G
|
XP_011529153.1:p.Thr882=
|
|
XM_011530849.2:c.5088A>G
|
XP_011529151.2:p.Thr1696=
|
|
XM_017029259.2:c.5079A>G
|
XP_016884748.1:p.Thr1693=
|
|
XM_017029260.1:c.5070A>G
|
XP_016884749.1:p.Thr1690=
|
|
XM_017029263.2:c.3408A>G
|
XP_016884752.1:p.Thr1136=
|
|
NM_000495.5:c.5055A>G
|
NP_000486.1:p.Thr1685=
|
|
NM_033380.3:c.5073A>G
MANE Select
|
NP_203699.1:p.Thr1691=
|
|