ENST00000328300.11:c.4814T>C
MANE Select
|
ENSP00000331902.7:p.Phe1605Ser
|
|
ENST00000361603.7:c.4796T>C
|
ENSP00000354505.2:p.Phe1599Ser
|
|
ENST00000510690.2:n.1308T>C
|
|
|
ENST00000644079.1:n.1300T>C
|
|
|
ENST00000328300.10:c.4814T>C
|
ENSP00000331902.6:p.Phe1605Ser
|
|
ENST00000361603.6:c.4796T>C
|
ENSP00000354505.2:p.Phe1599Ser
|
|
ENST00000504541.1:c.212T>C
|
ENSP00000424845.1:p.Phe71Ser
|
|
ENST00000515658.1:c.325-1383T>C
|
|
|
NM_000495.4:c.4796T>C
|
NP_000486.1:p.Phe1599Ser
|
|
NM_033380.2:c.4814T>C
|
NP_203699.1:p.Phe1605Ser
|
|
XM_005262070.2:c.4805T>C
|
XP_005262127.1:p.Phe1602Ser
|
|
XM_006724616.2:c.4814T>C
|
XP_006724679.1:p.Phe1605Ser
|
|
XM_011530849.1:c.4490T>C
|
XP_011529151.1:p.Phe1497Ser
|
|
XM_011530851.1:c.2387T>C
|
XP_011529153.1:p.Phe796Ser
|
|
XM_011530849.2:c.4829T>C
|
XP_011529151.2:p.Phe1610Ser
|
|
XM_017029259.2:c.4820T>C
|
XP_016884748.1:p.Phe1607Ser
|
|
XM_017029260.1:c.4811T>C
|
XP_016884749.1:p.Phe1604Ser
|
|
XM_017029263.2:c.3149T>C
|
XP_016884752.1:p.Phe1050Ser
|
|
NM_000495.5:c.4796T>C
|
NP_000486.1:p.Phe1599Ser
|
|
NM_033380.3:c.4814T>C
MANE Select
|
NP_203699.1:p.Phe1605Ser
|
|