ENST00000302850.10:c.2935C>A
MANE Select
|
ENSP00000303830.4:p.Leu979Met
|
|
ENST00000302850.9:c.2935C>A
|
ENSP00000303830.4:p.Leu979Met
|
|
ENST00000341500.9:c.2899C>A
|
ENSP00000342838.4:p.Leu967Met
|
|
NM_000208.2:c.2935C>A
|
NP_000199.2:p.Leu979Met
|
|
NM_000208.3:c.2935C>A
|
NP_000199.2:p.Leu979Met
|
|
NM_001079817.1:c.2899C>A
|
NP_001073285.1:p.Leu967Met
|
|
NM_001079817.2:c.2899C>A
|
NP_001073285.1:p.Leu967Met
|
|
XM_011527988.1:c.3010C>A
|
XP_011526290.1:p.Leu1004Met
|
|
XM_011527989.1:c.2974C>A
|
XP_011526291.1:p.Leu992Met
|
|
XM_011527988.2:c.2932C>A
|
XP_011526290.2:p.Leu978Met
|
|
XM_011527989.3:c.2896C>A
|
XP_011526291.2:p.Leu966Met
|
|
NM_000208.4:c.2935C>A
MANE Select
|
NP_000199.2:p.Leu979Met
|
|
NM_001079817.3:c.2899C>A
|
NP_001073285.1:p.Leu967Met
|
|