ENST00000328300.11:c.4349A>T
MANE Select
|
ENSP00000331902.7:p.Asp1450Val
|
|
ENST00000361603.7:c.4331A>T
|
ENSP00000354505.2:p.Asp1444Val
|
|
ENST00000510690.2:n.843A>T
|
|
|
ENST00000328300.10:c.4349A>T
|
ENSP00000331902.6:p.Asp1450Val
|
|
ENST00000361603.6:c.4331A>T
|
ENSP00000354505.2:p.Asp1444Val
|
|
ENST00000515658.1:c.145A>T
|
|
|
NM_000495.4:c.4331A>T
|
NP_000486.1:p.Asp1444Val
|
|
NM_033380.2:c.4349A>T
|
NP_203699.1:p.Asp1450Val
|
|
XM_005262070.2:c.4340A>T
|
XP_005262127.1:p.Asp1447Val
|
|
XM_006724616.2:c.4349A>T
|
XP_006724679.1:p.Asp1450Val
|
|
XM_011530849.1:c.4025A>T
|
XP_011529151.1:p.Asp1342Val
|
|
XM_011530851.1:c.1922A>T
|
XP_011529153.1:p.Asp641Val
|
|
XM_011530849.2:c.4364A>T
|
XP_011529151.2:p.Asp1455Val
|
|
XM_017029259.2:c.4355A>T
|
XP_016884748.1:p.Asp1452Val
|
|
XM_017029260.1:c.4346A>T
|
XP_016884749.1:p.Asp1449Val
|
|
XM_017029263.2:c.2684A>T
|
XP_016884752.1:p.Asp895Val
|
|
NM_000495.5:c.4331A>T
|
NP_000486.1:p.Asp1444Val
|
|
NM_033380.3:c.4349A>T
MANE Select
|
NP_203699.1:p.Asp1450Val
|
|