ENST00000328300.11:c.4522G>C
MANE Select
|
ENSP00000331902.7:p.Asp1508His
|
|
ENST00000361603.7:c.4504G>C
|
ENSP00000354505.2:p.Asp1502His
|
|
ENST00000510690.2:n.1016G>C
|
|
|
ENST00000328300.10:c.4522G>C
|
ENSP00000331902.6:p.Asp1508His
|
|
ENST00000361603.6:c.4504G>C
|
ENSP00000354505.2:p.Asp1502His
|
|
ENST00000515658.1:c.318G>C
|
|
|
NM_000495.4:c.4504G>C
|
NP_000486.1:p.Asp1502His
|
|
NM_033380.2:c.4522G>C
|
NP_203699.1:p.Asp1508His
|
|
XM_005262070.2:c.4513G>C
|
XP_005262127.1:p.Asp1505His
|
|
XM_006724616.2:c.4522G>C
|
XP_006724679.1:p.Asp1508His
|
|
XM_011530849.1:c.4198G>C
|
XP_011529151.1:p.Asp1400His
|
|
XM_011530851.1:c.2095G>C
|
XP_011529153.1:p.Asp699His
|
|
XM_011530849.2:c.4537G>C
|
XP_011529151.2:p.Asp1513His
|
|
XM_017029259.2:c.4528G>C
|
XP_016884748.1:p.Asp1510His
|
|
XM_017029260.1:c.4519G>C
|
XP_016884749.1:p.Asp1507His
|
|
XM_017029263.2:c.2857G>C
|
XP_016884752.1:p.Asp953His
|
|
NM_000495.5:c.4504G>C
|
NP_000486.1:p.Asp1502His
|
|
NM_033380.3:c.4522G>C
MANE Select
|
NP_203699.1:p.Asp1508His
|
|