ENST00000328300.11:c.4175T>A
MANE Select
|
ENSP00000331902.7:p.Leu1392Gln
|
|
ENST00000361603.7:c.4157T>A
|
ENSP00000354505.2:p.Leu1386Gln
|
|
ENST00000510690.2:n.669T>A
|
|
|
ENST00000328300.10:c.4175T>A
|
ENSP00000331902.6:p.Leu1392Gln
|
|
ENST00000361603.6:c.4157T>A
|
ENSP00000354505.2:p.Leu1386Gln
|
|
ENST00000489230.1:n.578T>A
|
|
|
NM_000495.4:c.4157T>A
|
NP_000486.1:p.Leu1386Gln
|
|
NM_033380.2:c.4175T>A
|
NP_203699.1:p.Leu1392Gln
|
|
XM_005262070.2:c.4166T>A
|
XP_005262127.1:p.Leu1389Gln
|
|
XM_006724616.2:c.4175T>A
|
XP_006724679.1:p.Leu1392Gln
|
|
XM_011530849.1:c.3851T>A
|
XP_011529151.1:p.Leu1284Gln
|
|
XM_011530851.1:c.1748T>A
|
XP_011529153.1:p.Leu583Gln
|
|
XM_011530849.2:c.4190T>A
|
XP_011529151.2:p.Leu1397Gln
|
|
XM_017029259.2:c.4181T>A
|
XP_016884748.1:p.Leu1394Gln
|
|
XM_017029260.1:c.4172T>A
|
XP_016884749.1:p.Leu1391Gln
|
|
XM_017029263.2:c.2510T>A
|
XP_016884752.1:p.Leu837Gln
|
|
NM_000495.5:c.4157T>A
|
NP_000486.1:p.Leu1386Gln
|
|
NM_033380.3:c.4175T>A
MANE Select
|
NP_203699.1:p.Leu1392Gln
|
|