ENST00000302850.10:c.3922_3924del
MANE Select
|
ENSP00000303830.4:p.Glu1308del
|
|
ENST00000302850.9:c.3922_3924del
|
ENSP00000303830.4:p.Glu1308del
|
|
ENST00000341500.9:c.3886_3888del
|
ENSP00000342838.4:p.Glu1296del
|
|
NM_000208.2:c.3922_3924del
|
NP_000199.2:p.Glu1308del
|
|
NM_000208.3:c.3922_3924del
|
NP_000199.2:p.Glu1308del
|
|
NM_001079817.1:c.3886_3888del
|
NP_001073285.1:p.Glu1296del
|
|
NM_001079817.2:c.3886_3888del
|
NP_001073285.1:p.Glu1296del
|
|
XM_011527988.1:c.3997_3999del
|
XP_011526290.1:p.Glu1333del
|
|
XM_011527989.1:c.3961_3963del
|
XP_011526291.1:p.Glu1321del
|
|
XM_011527988.2:c.3919_3921del
|
XP_011526290.2:p.Glu1307del
|
|
XM_011527989.3:c.3883_3885del
|
XP_011526291.2:p.Glu1295del
|
|
NM_000208.4:c.3922_3924del
MANE Select
|
NP_000199.2:p.Glu1308del
|
|
NM_001079817.3:c.3886_3888del
|
NP_001073285.1:p.Glu1296del
|
|