ENST00000328300.11:c.4789G>C
MANE Select
|
ENSP00000331902.7:p.Asp1597His
|
|
ENST00000361603.7:c.4771G>C
|
ENSP00000354505.2:p.Asp1591His
|
|
ENST00000510690.2:n.1283G>C
|
|
|
ENST00000644079.1:n.1275G>C
|
|
|
ENST00000328300.10:c.4789G>C
|
ENSP00000331902.6:p.Asp1597His
|
|
ENST00000361603.6:c.4771G>C
|
ENSP00000354505.2:p.Asp1591His
|
|
ENST00000504541.1:c.187G>C
|
ENSP00000424845.1:p.Asp63His
|
|
ENST00000515658.1:c.325-1408G>C
|
|
|
NM_000495.4:c.4771G>C
|
NP_000486.1:p.Asp1591His
|
|
NM_033380.2:c.4789G>C
|
NP_203699.1:p.Asp1597His
|
|
XM_005262070.2:c.4780G>C
|
XP_005262127.1:p.Asp1594His
|
|
XM_006724616.2:c.4789G>C
|
XP_006724679.1:p.Asp1597His
|
|
XM_011530849.1:c.4465G>C
|
XP_011529151.1:p.Asp1489His
|
|
XM_011530851.1:c.2362G>C
|
XP_011529153.1:p.Asp788His
|
|
XM_011530849.2:c.4804G>C
|
XP_011529151.2:p.Asp1602His
|
|
XM_017029259.2:c.4795G>C
|
XP_016884748.1:p.Asp1599His
|
|
XM_017029260.1:c.4786G>C
|
XP_016884749.1:p.Asp1596His
|
|
XM_017029263.2:c.3124G>C
|
XP_016884752.1:p.Asp1042His
|
|
NM_000495.5:c.4771G>C
|
NP_000486.1:p.Asp1591His
|
|
NM_033380.3:c.4789G>C
MANE Select
|
NP_203699.1:p.Asp1597His
|
|