ENST00000328300.11:c.4359A>G
MANE Select
|
ENSP00000331902.7:p.Gln1453=
|
|
ENST00000361603.7:c.4341A>G
|
ENSP00000354505.2:p.Gln1447=
|
|
ENST00000510690.2:n.853A>G
|
|
|
ENST00000328300.10:c.4359A>G
|
ENSP00000331902.6:p.Gln1453=
|
|
ENST00000361603.6:c.4341A>G
|
ENSP00000354505.2:p.Gln1447=
|
|
ENST00000515658.1:c.155A>G
|
|
|
NM_000495.4:c.4341A>G
|
NP_000486.1:p.Gln1447=
|
|
NM_033380.2:c.4359A>G
|
NP_203699.1:p.Gln1453=
|
|
XM_005262070.2:c.4350A>G
|
XP_005262127.1:p.Gln1450=
|
|
XM_006724616.2:c.4359A>G
|
XP_006724679.1:p.Gln1453=
|
|
XM_011530849.1:c.4035A>G
|
XP_011529151.1:p.Gln1345=
|
|
XM_011530851.1:c.1932A>G
|
XP_011529153.1:p.Gln644=
|
|
XM_011530849.2:c.4374A>G
|
XP_011529151.2:p.Gln1458=
|
|
XM_017029259.2:c.4365A>G
|
XP_016884748.1:p.Gln1455=
|
|
XM_017029260.1:c.4356A>G
|
XP_016884749.1:p.Gln1452=
|
|
XM_017029263.2:c.2694A>G
|
XP_016884752.1:p.Gln898=
|
|
NM_000495.5:c.4341A>G
|
NP_000486.1:p.Gln1447=
|
|
NM_033380.3:c.4359A>G
MANE Select
|
NP_203699.1:p.Gln1453=
|
|