ENST00000328300.11:c.4074T>G
MANE Select
|
ENSP00000331902.7:p.Leu1358=
|
|
ENST00000361603.7:c.4056T>G
|
ENSP00000354505.2:p.Leu1352=
|
|
ENST00000510690.2:n.568T>G
|
|
|
ENST00000328300.10:c.4074T>G
|
ENSP00000331902.6:p.Leu1358=
|
|
ENST00000361603.6:c.4056T>G
|
ENSP00000354505.2:p.Leu1352=
|
|
ENST00000489230.1:n.477T>G
|
|
|
NM_000495.4:c.4056T>G
|
NP_000486.1:p.Leu1352=
|
|
NM_033380.2:c.4074T>G
|
NP_203699.1:p.Leu1358=
|
|
XM_005262070.2:c.4065T>G
|
XP_005262127.1:p.Leu1355=
|
|
XM_006724616.2:c.4074T>G
|
XP_006724679.1:p.Leu1358=
|
|
XM_011530849.1:c.3750T>G
|
XP_011529151.1:p.Leu1250=
|
|
XM_011530851.1:c.1647T>G
|
XP_011529153.1:p.Leu549=
|
|
XM_011530849.2:c.4089T>G
|
XP_011529151.2:p.Leu1363=
|
|
XM_017029259.2:c.4080T>G
|
XP_016884748.1:p.Leu1360=
|
|
XM_017029260.1:c.4071T>G
|
XP_016884749.1:p.Leu1357=
|
|
XM_017029263.2:c.2409T>G
|
XP_016884752.1:p.Leu803=
|
|
NM_000495.5:c.4056T>G
|
NP_000486.1:p.Leu1352=
|
|
NM_033380.3:c.4074T>G
MANE Select
|
NP_203699.1:p.Leu1358=
|
|