ENST00000328300.11:c.4814T>A
MANE Select
|
ENSP00000331902.7:p.Phe1605Tyr
|
|
ENST00000361603.7:c.4796T>A
|
ENSP00000354505.2:p.Phe1599Tyr
|
|
ENST00000510690.2:n.1308T>A
|
|
|
ENST00000644079.1:n.1300T>A
|
|
|
ENST00000328300.10:c.4814T>A
|
ENSP00000331902.6:p.Phe1605Tyr
|
|
ENST00000361603.6:c.4796T>A
|
ENSP00000354505.2:p.Phe1599Tyr
|
|
ENST00000504541.1:c.212T>A
|
ENSP00000424845.1:p.Phe71Tyr
|
|
ENST00000515658.1:c.325-1383T>A
|
|
|
NM_000495.4:c.4796T>A
|
NP_000486.1:p.Phe1599Tyr
|
|
NM_033380.2:c.4814T>A
|
NP_203699.1:p.Phe1605Tyr
|
|
XM_005262070.2:c.4805T>A
|
XP_005262127.1:p.Phe1602Tyr
|
|
XM_006724616.2:c.4814T>A
|
XP_006724679.1:p.Phe1605Tyr
|
|
XM_011530849.1:c.4490T>A
|
XP_011529151.1:p.Phe1497Tyr
|
|
XM_011530851.1:c.2387T>A
|
XP_011529153.1:p.Phe796Tyr
|
|
XM_011530849.2:c.4829T>A
|
XP_011529151.2:p.Phe1610Tyr
|
|
XM_017029259.2:c.4820T>A
|
XP_016884748.1:p.Phe1607Tyr
|
|
XM_017029260.1:c.4811T>A
|
XP_016884749.1:p.Phe1604Tyr
|
|
XM_017029263.2:c.3149T>A
|
XP_016884752.1:p.Phe1050Tyr
|
|
NM_000495.5:c.4796T>A
|
NP_000486.1:p.Phe1599Tyr
|
|
NM_033380.3:c.4814T>A
MANE Select
|
NP_203699.1:p.Phe1605Tyr
|
|