ENST00000328300.11:c.4321C>G
MANE Select
|
ENSP00000331902.7:p.Arg1441Gly
|
|
ENST00000361603.7:c.4303C>G
|
ENSP00000354505.2:p.Arg1435Gly
|
|
ENST00000510690.2:n.815C>G
|
|
|
ENST00000328300.10:c.4321C>G
|
ENSP00000331902.6:p.Arg1441Gly
|
|
ENST00000361603.6:c.4303C>G
|
ENSP00000354505.2:p.Arg1435Gly
|
|
ENST00000489230.1:n.724C>G
|
|
|
ENST00000515658.1:c.117C>G
|
|
|
NM_000495.4:c.4303C>G
|
NP_000486.1:p.Arg1435Gly
|
|
NM_033380.2:c.4321C>G
|
NP_203699.1:p.Arg1441Gly
|
|
XM_005262070.2:c.4312C>G
|
XP_005262127.1:p.Arg1438Gly
|
|
XM_006724616.2:c.4321C>G
|
XP_006724679.1:p.Arg1441Gly
|
|
XM_011530849.1:c.3997C>G
|
XP_011529151.1:p.Arg1333Gly
|
|
XM_011530851.1:c.1894C>G
|
XP_011529153.1:p.Arg632Gly
|
|
XM_011530849.2:c.4336C>G
|
XP_011529151.2:p.Arg1446Gly
|
|
XM_017029259.2:c.4327C>G
|
XP_016884748.1:p.Arg1443Gly
|
|
XM_017029260.1:c.4318C>G
|
XP_016884749.1:p.Arg1440Gly
|
|
XM_017029263.2:c.2656C>G
|
XP_016884752.1:p.Arg886Gly
|
|
NM_000495.5:c.4303C>G
|
NP_000486.1:p.Arg1435Gly
|
|
NM_033380.3:c.4321C>G
MANE Select
|
NP_203699.1:p.Arg1441Gly
|
|