ENST00000328300.11:c.4041T>C
MANE Select
|
ENSP00000331902.7:p.Pro1347=
|
|
ENST00000361603.7:c.4023T>C
|
ENSP00000354505.2:p.Pro1341=
|
|
ENST00000510690.2:n.535T>C
|
|
|
ENST00000328300.10:c.4041T>C
|
ENSP00000331902.6:p.Pro1347=
|
|
ENST00000361603.6:c.4023T>C
|
ENSP00000354505.2:p.Pro1341=
|
|
ENST00000489230.1:n.444T>C
|
|
|
NM_000495.4:c.4023T>C
|
NP_000486.1:p.Pro1341=
|
|
NM_033380.2:c.4041T>C
|
NP_203699.1:p.Pro1347=
|
|
XM_005262070.2:c.4032T>C
|
XP_005262127.1:p.Pro1344=
|
|
XM_006724616.2:c.4041T>C
|
XP_006724679.1:p.Pro1347=
|
|
XM_011530849.1:c.3717T>C
|
XP_011529151.1:p.Pro1239=
|
|
XM_011530851.1:c.1614T>C
|
XP_011529153.1:p.Pro538=
|
|
XM_011530849.2:c.4056T>C
|
XP_011529151.2:p.Pro1352=
|
|
XM_017029259.2:c.4047T>C
|
XP_016884748.1:p.Pro1349=
|
|
XM_017029260.1:c.4038T>C
|
XP_016884749.1:p.Pro1346=
|
|
XM_017029263.2:c.2376T>C
|
XP_016884752.1:p.Pro792=
|
|
NM_000495.5:c.4023T>C
|
NP_000486.1:p.Pro1341=
|
|
NM_033380.3:c.4041T>C
MANE Select
|
NP_203699.1:p.Pro1347=
|
|