ENST00000328300.11:c.4742C>A
MANE Select
|
ENSP00000331902.7:p.Ala1581Glu
|
|
ENST00000361603.7:c.4724C>A
|
ENSP00000354505.2:p.Ala1575Glu
|
|
ENST00000510690.2:n.1236C>A
|
|
|
ENST00000644079.1:n.1228C>A
|
|
|
ENST00000328300.10:c.4742C>A
|
ENSP00000331902.6:p.Ala1581Glu
|
|
ENST00000361603.6:c.4724C>A
|
ENSP00000354505.2:p.Ala1575Glu
|
|
ENST00000504541.1:c.140C>A
|
ENSP00000424845.1:p.Ala47Glu
|
|
ENST00000515658.1:c.325-1455C>A
|
|
|
NM_000495.4:c.4724C>A
|
NP_000486.1:p.Ala1575Glu
|
|
NM_033380.2:c.4742C>A
|
NP_203699.1:p.Ala1581Glu
|
|
XM_005262070.2:c.4733C>A
|
XP_005262127.1:p.Ala1578Glu
|
|
XM_006724616.2:c.4742C>A
|
XP_006724679.1:p.Ala1581Glu
|
|
XM_011530849.1:c.4418C>A
|
XP_011529151.1:p.Ala1473Glu
|
|
XM_011530851.1:c.2315C>A
|
XP_011529153.1:p.Ala772Glu
|
|
XM_011530849.2:c.4757C>A
|
XP_011529151.2:p.Ala1586Glu
|
|
XM_017029259.2:c.4748C>A
|
XP_016884748.1:p.Ala1583Glu
|
|
XM_017029260.1:c.4739C>A
|
XP_016884749.1:p.Ala1580Glu
|
|
XM_017029263.2:c.3077C>A
|
XP_016884752.1:p.Ala1026Glu
|
|
NM_000495.5:c.4724C>A
|
NP_000486.1:p.Ala1575Glu
|
|
NM_033380.3:c.4742C>A
MANE Select
|
NP_203699.1:p.Ala1581Glu
|
|