ENST00000328300.11:c.4068G>C
MANE Select
|
ENSP00000331902.7:p.Pro1356=
|
|
ENST00000361603.7:c.4050G>C
|
ENSP00000354505.2:p.Pro1350=
|
|
ENST00000510690.2:n.562G>C
|
|
|
ENST00000328300.10:c.4068G>C
|
ENSP00000331902.6:p.Pro1356=
|
|
ENST00000361603.6:c.4050G>C
|
ENSP00000354505.2:p.Pro1350=
|
|
ENST00000489230.1:n.471G>C
|
|
|
NM_000495.4:c.4050G>C
|
NP_000486.1:p.Pro1350=
|
|
NM_033380.2:c.4068G>C
|
NP_203699.1:p.Pro1356=
|
|
XM_005262070.2:c.4059G>C
|
XP_005262127.1:p.Pro1353=
|
|
XM_006724616.2:c.4068G>C
|
XP_006724679.1:p.Pro1356=
|
|
XM_011530849.1:c.3744G>C
|
XP_011529151.1:p.Pro1248=
|
|
XM_011530851.1:c.1641G>C
|
XP_011529153.1:p.Pro547=
|
|
XM_011530849.2:c.4083G>C
|
XP_011529151.2:p.Pro1361=
|
|
XM_017029259.2:c.4074G>C
|
XP_016884748.1:p.Pro1358=
|
|
XM_017029260.1:c.4065G>C
|
XP_016884749.1:p.Pro1355=
|
|
XM_017029263.2:c.2403G>C
|
XP_016884752.1:p.Pro801=
|
|
NM_000495.5:c.4050G>C
|
NP_000486.1:p.Pro1350=
|
|
NM_033380.3:c.4068G>C
MANE Select
|
NP_203699.1:p.Pro1356=
|
|