ENST00000302850.10:c.3145G>T
MANE Select
|
ENSP00000303830.4:p.Glu1049Ter
|
|
ENST00000302850.9:c.3145G>T
|
ENSP00000303830.4:p.Glu1049Ter
|
|
ENST00000341500.9:c.3109G>T
|
ENSP00000342838.4:p.Glu1037Ter
|
|
NM_000208.2:c.3145G>T
|
NP_000199.2:p.Glu1049Ter
|
|
NM_000208.3:c.3145G>T
|
NP_000199.2:p.Glu1049Ter
|
|
NM_001079817.1:c.3109G>T
|
NP_001073285.1:p.Glu1037Ter
|
|
NM_001079817.2:c.3109G>T
|
NP_001073285.1:p.Glu1037Ter
|
|
XM_011527988.1:c.3220G>T
|
XP_011526290.1:p.Glu1074Ter
|
|
XM_011527989.1:c.3184G>T
|
XP_011526291.1:p.Glu1062Ter
|
|
XM_011527988.2:c.3142G>T
|
XP_011526290.2:p.Glu1048Ter
|
|
XM_011527989.3:c.3106G>T
|
XP_011526291.2:p.Glu1036Ter
|
|
NM_000208.4:c.3145G>T
MANE Select
|
NP_000199.2:p.Glu1049Ter
|
|
NM_001079817.3:c.3109G>T
|
NP_001073285.1:p.Glu1037Ter
|
|