ENST00000328300.11:c.4795C>A
MANE Select
|
ENSP00000331902.7:p.Leu1599Met
|
|
ENST00000361603.7:c.4777C>A
|
ENSP00000354505.2:p.Leu1593Met
|
|
ENST00000510690.2:n.1289C>A
|
|
|
ENST00000644079.1:n.1281C>A
|
|
|
ENST00000328300.10:c.4795C>A
|
ENSP00000331902.6:p.Leu1599Met
|
|
ENST00000361603.6:c.4777C>A
|
ENSP00000354505.2:p.Leu1593Met
|
|
ENST00000504541.1:c.193C>A
|
ENSP00000424845.1:p.Leu65Met
|
|
ENST00000515658.1:c.325-1402C>A
|
|
|
NM_000495.4:c.4777C>A
|
NP_000486.1:p.Leu1593Met
|
|
NM_033380.2:c.4795C>A
|
NP_203699.1:p.Leu1599Met
|
|
XM_005262070.2:c.4786C>A
|
XP_005262127.1:p.Leu1596Met
|
|
XM_006724616.2:c.4795C>A
|
XP_006724679.1:p.Leu1599Met
|
|
XM_011530849.1:c.4471C>A
|
XP_011529151.1:p.Leu1491Met
|
|
XM_011530851.1:c.2368C>A
|
XP_011529153.1:p.Leu790Met
|
|
XM_011530849.2:c.4810C>A
|
XP_011529151.2:p.Leu1604Met
|
|
XM_017029259.2:c.4801C>A
|
XP_016884748.1:p.Leu1601Met
|
|
XM_017029260.1:c.4792C>A
|
XP_016884749.1:p.Leu1598Met
|
|
XM_017029263.2:c.3130C>A
|
XP_016884752.1:p.Leu1044Met
|
|
NM_000495.5:c.4777C>A
|
NP_000486.1:p.Leu1593Met
|
|
NM_033380.3:c.4795C>A
MANE Select
|
NP_203699.1:p.Leu1599Met
|
|