ENST00000328300.11:c.3813A>G
MANE Select
|
ENSP00000331902.7:p.Leu1271=
|
|
ENST00000361603.7:c.3795A>G
|
ENSP00000354505.2:p.Leu1265=
|
|
ENST00000510690.2:n.307A>G
|
|
|
ENST00000328300.10:c.3813A>G
|
ENSP00000331902.6:p.Leu1271=
|
|
ENST00000361603.6:c.3795A>G
|
ENSP00000354505.2:p.Leu1265=
|
|
ENST00000489230.1:n.216A>G
|
|
|
ENST00000510690.1:n.307A>G
|
|
|
NM_000495.4:c.3795A>G
|
NP_000486.1:p.Leu1265=
|
|
NM_033380.2:c.3813A>G
|
NP_203699.1:p.Leu1271=
|
|
XM_005262070.2:c.3804A>G
|
XP_005262127.1:p.Leu1268=
|
|
XM_006724616.2:c.3813A>G
|
XP_006724679.1:p.Leu1271=
|
|
XM_011530849.1:c.3489A>G
|
XP_011529151.1:p.Leu1163=
|
|
XM_011530851.1:c.1386A>G
|
XP_011529153.1:p.Leu462=
|
|
XM_011530849.2:c.3828A>G
|
XP_011529151.2:p.Leu1276=
|
|
XM_017029259.2:c.3819A>G
|
XP_016884748.1:p.Leu1273=
|
|
XM_017029260.1:c.3810A>G
|
XP_016884749.1:p.Leu1270=
|
|
XM_017029261.1:c.3828A>G
|
XP_016884750.1:p.Leu1276=
|
|
XM_017029263.2:c.2148A>G
|
XP_016884752.1:p.Leu716=
|
|
NM_000495.5:c.3795A>G
|
NP_000486.1:p.Leu1265=
|
|
NM_033380.3:c.3813A>G
MANE Select
|
NP_203699.1:p.Leu1271=
|
|