ENST00000302850.10:c.3952G>T
MANE Select
|
ENSP00000303830.4:p.Glu1318Ter
|
|
ENST00000302850.9:c.3952G>T
|
ENSP00000303830.4:p.Glu1318Ter
|
|
ENST00000341500.9:c.3916G>T
|
ENSP00000342838.4:p.Glu1306Ter
|
|
NM_000208.2:c.3952G>T
|
NP_000199.2:p.Glu1318Ter
|
|
NM_000208.3:c.3952G>T
|
NP_000199.2:p.Glu1318Ter
|
|
NM_001079817.1:c.3916G>T
|
NP_001073285.1:p.Glu1306Ter
|
|
NM_001079817.2:c.3916G>T
|
NP_001073285.1:p.Glu1306Ter
|
|
XM_011527988.1:c.4027G>T
|
XP_011526290.1:p.Glu1343Ter
|
|
XM_011527989.1:c.3991G>T
|
XP_011526291.1:p.Glu1331Ter
|
|
XM_011527988.2:c.3949G>T
|
XP_011526290.2:p.Glu1317Ter
|
|
XM_011527989.3:c.3913G>T
|
XP_011526291.2:p.Glu1305Ter
|
|
NM_000208.4:c.3952G>T
MANE Select
|
NP_000199.2:p.Glu1318Ter
|
|
NM_001079817.3:c.3916G>T
|
NP_001073285.1:p.Glu1306Ter
|
|