ENST00000328300.11:c.4719T>C
MANE Select
|
ENSP00000331902.7:p.Cys1573=
|
|
ENST00000361603.7:c.4701T>C
|
ENSP00000354505.2:p.Cys1567=
|
|
ENST00000510690.2:n.1213T>C
|
|
|
ENST00000644079.1:n.1205T>C
|
|
|
ENST00000328300.10:c.4719T>C
|
ENSP00000331902.6:p.Cys1573=
|
|
ENST00000361603.6:c.4701T>C
|
ENSP00000354505.2:p.Cys1567=
|
|
ENST00000504541.1:c.117T>C
|
ENSP00000424845.1:p.Cys39=
|
|
ENST00000515658.1:c.325-1478T>C
|
|
|
NM_000495.4:c.4701T>C
|
NP_000486.1:p.Cys1567=
|
|
NM_033380.2:c.4719T>C
|
NP_203699.1:p.Cys1573=
|
|
XM_005262070.2:c.4710T>C
|
XP_005262127.1:p.Cys1570=
|
|
XM_006724616.2:c.4719T>C
|
XP_006724679.1:p.Cys1573=
|
|
XM_011530849.1:c.4395T>C
|
XP_011529151.1:p.Cys1465=
|
|
XM_011530851.1:c.2292T>C
|
XP_011529153.1:p.Cys764=
|
|
XM_011530849.2:c.4734T>C
|
XP_011529151.2:p.Cys1578=
|
|
XM_017029259.2:c.4725T>C
|
XP_016884748.1:p.Cys1575=
|
|
XM_017029260.1:c.4716T>C
|
XP_016884749.1:p.Cys1572=
|
|
XM_017029263.2:c.3054T>C
|
XP_016884752.1:p.Cys1018=
|
|
NM_000495.5:c.4701T>C
|
NP_000486.1:p.Cys1567=
|
|
NM_033380.3:c.4719T>C
MANE Select
|
NP_203699.1:p.Cys1573=
|
|