ENST00000328300.11:c.4772A>C
MANE Select
|
ENSP00000331902.7:p.His1591Pro
|
|
ENST00000361603.7:c.4754A>C
|
ENSP00000354505.2:p.His1585Pro
|
|
ENST00000510690.2:n.1266A>C
|
|
|
ENST00000644079.1:n.1258A>C
|
|
|
ENST00000328300.10:c.4772A>C
|
ENSP00000331902.6:p.His1591Pro
|
|
ENST00000361603.6:c.4754A>C
|
ENSP00000354505.2:p.His1585Pro
|
|
ENST00000504541.1:c.170A>C
|
ENSP00000424845.1:p.His57Pro
|
|
ENST00000515658.1:c.325-1425A>C
|
|
|
NM_000495.4:c.4754A>C
|
NP_000486.1:p.His1585Pro
|
|
NM_033380.2:c.4772A>C
|
NP_203699.1:p.His1591Pro
|
|
XM_005262070.2:c.4763A>C
|
XP_005262127.1:p.His1588Pro
|
|
XM_006724616.2:c.4772A>C
|
XP_006724679.1:p.His1591Pro
|
|
XM_011530849.1:c.4448A>C
|
XP_011529151.1:p.His1483Pro
|
|
XM_011530851.1:c.2345A>C
|
XP_011529153.1:p.His782Pro
|
|
XM_011530849.2:c.4787A>C
|
XP_011529151.2:p.His1596Pro
|
|
XM_017029259.2:c.4778A>C
|
XP_016884748.1:p.His1593Pro
|
|
XM_017029260.1:c.4769A>C
|
XP_016884749.1:p.His1590Pro
|
|
XM_017029263.2:c.3107A>C
|
XP_016884752.1:p.His1036Pro
|
|
NM_000495.5:c.4754A>C
|
NP_000486.1:p.His1585Pro
|
|
NM_033380.3:c.4772A>C
MANE Select
|
NP_203699.1:p.His1591Pro
|
|