ENST00000328300.11:c.4386C>A
MANE Select
|
ENSP00000331902.7:p.Ser1462=
|
|
ENST00000361603.7:c.4368C>A
|
ENSP00000354505.2:p.Ser1456=
|
|
ENST00000510690.2:n.880C>A
|
|
|
ENST00000328300.10:c.4386C>A
|
ENSP00000331902.6:p.Ser1462=
|
|
ENST00000361603.6:c.4368C>A
|
ENSP00000354505.2:p.Ser1456=
|
|
ENST00000515658.1:c.182C>A
|
|
|
NM_000495.4:c.4368C>A
|
NP_000486.1:p.Ser1456=
|
|
NM_033380.2:c.4386C>A
|
NP_203699.1:p.Ser1462=
|
|
XM_005262070.2:c.4377C>A
|
XP_005262127.1:p.Ser1459=
|
|
XM_006724616.2:c.4386C>A
|
XP_006724679.1:p.Ser1462=
|
|
XM_011530849.1:c.4062C>A
|
XP_011529151.1:p.Ser1354=
|
|
XM_011530851.1:c.1959C>A
|
XP_011529153.1:p.Ser653=
|
|
XM_011530849.2:c.4401C>A
|
XP_011529151.2:p.Ser1467=
|
|
XM_017029259.2:c.4392C>A
|
XP_016884748.1:p.Ser1464=
|
|
XM_017029260.1:c.4383C>A
|
XP_016884749.1:p.Ser1461=
|
|
XM_017029263.2:c.2721C>A
|
XP_016884752.1:p.Ser907=
|
|
NM_000495.5:c.4368C>A
|
NP_000486.1:p.Ser1456=
|
|
NM_033380.3:c.4386C>A
MANE Select
|
NP_203699.1:p.Ser1462=
|
|