ENST00000302850.10:c.2902T>A
MANE Select
|
ENSP00000303830.4:p.Phe968Ile
|
|
ENST00000302850.9:c.2902T>A
|
ENSP00000303830.4:p.Phe968Ile
|
|
ENST00000341500.9:c.2866T>A
|
ENSP00000342838.4:p.Phe956Ile
|
|
NM_000208.2:c.2902T>A
|
NP_000199.2:p.Phe968Ile
|
|
NM_000208.3:c.2902T>A
|
NP_000199.2:p.Phe968Ile
|
|
NM_001079817.1:c.2866T>A
|
NP_001073285.1:p.Phe956Ile
|
|
NM_001079817.2:c.2866T>A
|
NP_001073285.1:p.Phe956Ile
|
|
XM_011527988.1:c.2977T>A
|
XP_011526290.1:p.Phe993Ile
|
|
XM_011527989.1:c.2941T>A
|
XP_011526291.1:p.Phe981Ile
|
|
XM_011527988.2:c.2899T>A
|
XP_011526290.2:p.Phe967Ile
|
|
XM_011527989.3:c.2863T>A
|
XP_011526291.2:p.Phe955Ile
|
|
NM_000208.4:c.2902T>A
MANE Select
|
NP_000199.2:p.Phe968Ile
|
|
NM_001079817.3:c.2866T>A
|
NP_001073285.1:p.Phe956Ile
|
|