ENST00000328300.11:c.4314A>C
MANE Select
|
ENSP00000331902.7:p.Pro1438=
|
|
ENST00000361603.7:c.4296A>C
|
ENSP00000354505.2:p.Pro1432=
|
|
ENST00000510690.2:n.808A>C
|
|
|
ENST00000328300.10:c.4314A>C
|
ENSP00000331902.6:p.Pro1438=
|
|
ENST00000361603.6:c.4296A>C
|
ENSP00000354505.2:p.Pro1432=
|
|
ENST00000489230.1:n.717A>C
|
|
|
ENST00000515658.1:c.110A>C
|
|
|
NM_000495.4:c.4296A>C
|
NP_000486.1:p.Pro1432=
|
|
NM_033380.2:c.4314A>C
|
NP_203699.1:p.Pro1438=
|
|
XM_005262070.2:c.4305A>C
|
XP_005262127.1:p.Pro1435=
|
|
XM_006724616.2:c.4314A>C
|
XP_006724679.1:p.Pro1438=
|
|
XM_011530849.1:c.3990A>C
|
XP_011529151.1:p.Pro1330=
|
|
XM_011530851.1:c.1887A>C
|
XP_011529153.1:p.Pro629=
|
|
XM_011530849.2:c.4329A>C
|
XP_011529151.2:p.Pro1443=
|
|
XM_017029259.2:c.4320A>C
|
XP_016884748.1:p.Pro1440=
|
|
XM_017029260.1:c.4311A>C
|
XP_016884749.1:p.Pro1437=
|
|
XM_017029263.2:c.2649A>C
|
XP_016884752.1:p.Pro883=
|
|
NM_000495.5:c.4296A>C
|
NP_000486.1:p.Pro1432=
|
|
NM_033380.3:c.4314A>C
MANE Select
|
NP_203699.1:p.Pro1438=
|
|