ENST00000328300.11:c.3012A>T
MANE Select
|
ENSP00000331902.7:p.Pro1004=
|
|
ENST00000361603.7:c.3012A>T
|
ENSP00000354505.2:p.Pro1004=
|
|
ENST00000328300.10:c.3012A>T
|
ENSP00000331902.6:p.Pro1004=
|
|
ENST00000361603.6:c.3012A>T
|
ENSP00000354505.2:p.Pro1004=
|
|
ENST00000483338.1:n.2468A>T
|
|
|
ENST00000505728.1:c.245A>T
|
|
|
NM_000495.4:c.3012A>T
|
NP_000486.1:p.Pro1004=
|
|
NM_033380.2:c.3012A>T
|
NP_203699.1:p.Pro1004=
|
|
XM_005262070.2:c.3012A>T
|
XP_005262127.1:p.Pro1004=
|
|
XM_005262072.3:c.3012A>T
|
XP_005262129.1:p.Pro1004=
|
|
XM_006724616.2:c.3012A>T
|
XP_006724679.1:p.Pro1004=
|
|
XM_011530849.1:c.2688A>T
|
XP_011529151.1:p.Pro896=
|
|
XM_011530850.1:c.3012A>T
|
XP_011529152.1:p.Pro1004=
|
|
XM_011530851.1:c.585A>T
|
XP_011529153.1:p.Pro195=
|
|
XM_011530849.2:c.3027A>T
|
XP_011529151.2:p.Pro1009=
|
|
XM_017029259.2:c.3027A>T
|
XP_016884748.1:p.Pro1009=
|
|
XM_017029260.1:c.3027A>T
|
XP_016884749.1:p.Pro1009=
|
|
XM_017029261.1:c.3027A>T
|
XP_016884750.1:p.Pro1009=
|
|
XM_017029262.2:c.3027A>T
|
XP_016884751.1:p.Pro1009=
|
|
XM_017029263.2:c.1347A>T
|
XP_016884752.1:p.Pro449=
|
|
NM_000495.5:c.3012A>T
|
NP_000486.1:p.Pro1004=
|
|
NM_033380.3:c.3012A>T
MANE Select
|
NP_203699.1:p.Pro1004=
|
|