ENST00000328300.11:c.4322G>T
MANE Select
|
ENSP00000331902.7:p.Arg1441Leu
|
|
ENST00000361603.7:c.4304G>T
|
ENSP00000354505.2:p.Arg1435Leu
|
|
ENST00000510690.2:n.816G>T
|
|
|
ENST00000328300.10:c.4322G>T
|
ENSP00000331902.6:p.Arg1441Leu
|
|
ENST00000361603.6:c.4304G>T
|
ENSP00000354505.2:p.Arg1435Leu
|
|
ENST00000489230.1:n.725G>T
|
|
|
ENST00000515658.1:c.118G>T
|
|
|
NM_000495.4:c.4304G>T
|
NP_000486.1:p.Arg1435Leu
|
|
NM_033380.2:c.4322G>T
|
NP_203699.1:p.Arg1441Leu
|
|
XM_005262070.2:c.4313G>T
|
XP_005262127.1:p.Arg1438Leu
|
|
XM_006724616.2:c.4322G>T
|
XP_006724679.1:p.Arg1441Leu
|
|
XM_011530849.1:c.3998G>T
|
XP_011529151.1:p.Arg1333Leu
|
|
XM_011530851.1:c.1895G>T
|
XP_011529153.1:p.Arg632Leu
|
|
XM_011530849.2:c.4337G>T
|
XP_011529151.2:p.Arg1446Leu
|
|
XM_017029259.2:c.4328G>T
|
XP_016884748.1:p.Arg1443Leu
|
|
XM_017029260.1:c.4319G>T
|
XP_016884749.1:p.Arg1440Leu
|
|
XM_017029263.2:c.2657G>T
|
XP_016884752.1:p.Arg886Leu
|
|
NM_000495.5:c.4304G>T
|
NP_000486.1:p.Arg1435Leu
|
|
NM_033380.3:c.4322G>T
MANE Select
|
NP_203699.1:p.Arg1441Leu
|
|