ENST00000302850.10:c.4143T>G
MANE Select
|
ENSP00000303830.4:p.Pro1381=
|
|
ENST00000302850.9:c.4143T>G
|
ENSP00000303830.4:p.Pro1381=
|
|
ENST00000341500.9:c.4107T>G
|
ENSP00000342838.4:p.Pro1369=
|
|
NM_000208.2:c.4143T>G
|
NP_000199.2:p.Pro1381=
|
|
NM_000208.3:c.4143T>G
|
NP_000199.2:p.Pro1381=
|
|
NM_001079817.1:c.4107T>G
|
NP_001073285.1:p.Pro1369=
|
|
NM_001079817.2:c.4107T>G
|
NP_001073285.1:p.Pro1369=
|
|
XM_011527988.1:c.4218T>G
|
XP_011526290.1:p.Pro1406=
|
|
XM_011527989.1:c.4182T>G
|
XP_011526291.1:p.Pro1394=
|
|
XM_011527988.2:c.4140T>G
|
XP_011526290.2:p.Pro1380=
|
|
XM_011527989.3:c.4104T>G
|
XP_011526291.2:p.Pro1368=
|
|
NM_000208.4:c.4143T>G
MANE Select
|
NP_000199.2:p.Pro1381=
|
|
NM_001079817.3:c.4107T>G
|
NP_001073285.1:p.Pro1369=
|
|