ENST00000302850.10:c.3932C>A
MANE Select
|
ENSP00000303830.4:p.Ala1311Asp
|
|
ENST00000302850.9:c.3932C>A
|
ENSP00000303830.4:p.Ala1311Asp
|
|
ENST00000341500.9:c.3896C>A
|
ENSP00000342838.4:p.Ala1299Asp
|
|
NM_000208.2:c.3932C>A
|
NP_000199.2:p.Ala1311Asp
|
|
NM_000208.3:c.3932C>A
|
NP_000199.2:p.Ala1311Asp
|
|
NM_001079817.1:c.3896C>A
|
NP_001073285.1:p.Ala1299Asp
|
|
NM_001079817.2:c.3896C>A
|
NP_001073285.1:p.Ala1299Asp
|
|
XM_011527988.1:c.4007C>A
|
XP_011526290.1:p.Ala1336Asp
|
|
XM_011527989.1:c.3971C>A
|
XP_011526291.1:p.Ala1324Asp
|
|
XM_011527988.2:c.3929C>A
|
XP_011526290.2:p.Ala1310Asp
|
|
XM_011527989.3:c.3893C>A
|
XP_011526291.2:p.Ala1298Asp
|
|
NM_000208.4:c.3932C>A
MANE Select
|
NP_000199.2:p.Ala1311Asp
|
|
NM_001079817.3:c.3896C>A
|
NP_001073285.1:p.Ala1299Asp
|
|