ENST00000328300.11:c.4315G>A
MANE Select
|
ENSP00000331902.7:p.Gly1439Ser
|
|
ENST00000361603.7:c.4297G>A
|
ENSP00000354505.2:p.Gly1433Ser
|
|
ENST00000510690.2:n.809G>A
|
|
|
ENST00000328300.10:c.4315G>A
|
ENSP00000331902.6:p.Gly1439Ser
|
|
ENST00000361603.6:c.4297G>A
|
ENSP00000354505.2:p.Gly1433Ser
|
|
ENST00000489230.1:n.718G>A
|
|
|
ENST00000515658.1:c.111G>A
|
|
|
NM_000495.4:c.4297G>A
|
NP_000486.1:p.Gly1433Ser
|
|
NM_033380.2:c.4315G>A
|
NP_203699.1:p.Gly1439Ser
|
|
XM_005262070.2:c.4306G>A
|
XP_005262127.1:p.Gly1436Ser
|
|
XM_006724616.2:c.4315G>A
|
XP_006724679.1:p.Gly1439Ser
|
|
XM_011530849.1:c.3991G>A
|
XP_011529151.1:p.Gly1331Ser
|
|
XM_011530851.1:c.1888G>A
|
XP_011529153.1:p.Gly630Ser
|
|
XM_011530849.2:c.4330G>A
|
XP_011529151.2:p.Gly1444Ser
|
|
XM_017029259.2:c.4321G>A
|
XP_016884748.1:p.Gly1441Ser
|
|
XM_017029260.1:c.4312G>A
|
XP_016884749.1:p.Gly1438Ser
|
|
XM_017029263.2:c.2650G>A
|
XP_016884752.1:p.Gly884Ser
|
|
NM_000495.5:c.4297G>A
|
NP_000486.1:p.Gly1433Ser
|
|
NM_033380.3:c.4315G>A
MANE Select
|
NP_203699.1:p.Gly1439Ser
|
|