ENST00000328300.11:c.4563C>A
MANE Select
|
ENSP00000331902.7:p.Thr1521=
|
|
ENST00000361603.7:c.4545C>A
|
ENSP00000354505.2:p.Thr1515=
|
|
ENST00000510690.2:n.1057C>A
|
|
|
ENST00000328300.10:c.4563C>A
|
ENSP00000331902.6:p.Thr1521=
|
|
ENST00000361603.6:c.4545C>A
|
ENSP00000354505.2:p.Thr1515=
|
|
ENST00000515658.1:c.325-3515C>A
|
|
|
NM_000495.4:c.4545C>A
|
NP_000486.1:p.Thr1515=
|
|
NM_033380.2:c.4563C>A
|
NP_203699.1:p.Thr1521=
|
|
XM_005262070.2:c.4554C>A
|
XP_005262127.1:p.Thr1518=
|
|
XM_006724616.2:c.4563C>A
|
XP_006724679.1:p.Thr1521=
|
|
XM_011530849.1:c.4239C>A
|
XP_011529151.1:p.Thr1413=
|
|
XM_011530851.1:c.2136C>A
|
XP_011529153.1:p.Thr712=
|
|
XM_011530849.2:c.4578C>A
|
XP_011529151.2:p.Thr1526=
|
|
XM_017029259.2:c.4569C>A
|
XP_016884748.1:p.Thr1523=
|
|
XM_017029260.1:c.4560C>A
|
XP_016884749.1:p.Thr1520=
|
|
XM_017029263.2:c.2898C>A
|
XP_016884752.1:p.Thr966=
|
|
NM_000495.5:c.4545C>A
|
NP_000486.1:p.Thr1515=
|
|
NM_033380.3:c.4563C>A
MANE Select
|
NP_203699.1:p.Thr1521=
|
|