ENST00000328300.11:c.4811C>A
MANE Select
|
ENSP00000331902.7:p.Ser1604Tyr
|
|
ENST00000361603.7:c.4793C>A
|
ENSP00000354505.2:p.Ser1598Tyr
|
|
ENST00000510690.2:n.1305C>A
|
|
|
ENST00000644079.1:n.1297C>A
|
|
|
ENST00000328300.10:c.4811C>A
|
ENSP00000331902.6:p.Ser1604Tyr
|
|
ENST00000361603.6:c.4793C>A
|
ENSP00000354505.2:p.Ser1598Tyr
|
|
ENST00000504541.1:c.209C>A
|
ENSP00000424845.1:p.Ser70Tyr
|
|
ENST00000515658.1:c.325-1386C>A
|
|
|
NM_000495.4:c.4793C>A
|
NP_000486.1:p.Ser1598Tyr
|
|
NM_033380.2:c.4811C>A
|
NP_203699.1:p.Ser1604Tyr
|
|
XM_005262070.2:c.4802C>A
|
XP_005262127.1:p.Ser1601Tyr
|
|
XM_006724616.2:c.4811C>A
|
XP_006724679.1:p.Ser1604Tyr
|
|
XM_011530849.1:c.4487C>A
|
XP_011529151.1:p.Ser1496Tyr
|
|
XM_011530851.1:c.2384C>A
|
XP_011529153.1:p.Ser795Tyr
|
|
XM_011530849.2:c.4826C>A
|
XP_011529151.2:p.Ser1609Tyr
|
|
XM_017029259.2:c.4817C>A
|
XP_016884748.1:p.Ser1606Tyr
|
|
XM_017029260.1:c.4808C>A
|
XP_016884749.1:p.Ser1603Tyr
|
|
XM_017029263.2:c.3146C>A
|
XP_016884752.1:p.Ser1049Tyr
|
|
NM_000495.5:c.4793C>A
|
NP_000486.1:p.Ser1598Tyr
|
|
NM_033380.3:c.4811C>A
MANE Select
|
NP_203699.1:p.Ser1604Tyr
|
|