ENST00000302850.10:c.3035T>A
MANE Select
|
ENSP00000303830.4:p.Val1012Glu
|
|
ENST00000302850.9:c.3035T>A
|
ENSP00000303830.4:p.Val1012Glu
|
|
ENST00000341500.9:c.2999T>A
|
ENSP00000342838.4:p.Val1000Glu
|
|
NM_000208.2:c.3035T>A
|
NP_000199.2:p.Val1012Glu
|
|
NM_000208.3:c.3035T>A
|
NP_000199.2:p.Val1012Glu
|
|
NM_001079817.1:c.2999T>A
|
NP_001073285.1:p.Val1000Glu
|
|
NM_001079817.2:c.2999T>A
|
NP_001073285.1:p.Val1000Glu
|
|
XM_011527988.1:c.3110T>A
|
XP_011526290.1:p.Val1037Glu
|
|
XM_011527989.1:c.3074T>A
|
XP_011526291.1:p.Val1025Glu
|
|
XM_011527988.2:c.3032T>A
|
XP_011526290.2:p.Val1011Glu
|
|
XM_011527989.3:c.2996T>A
|
XP_011526291.2:p.Val999Glu
|
|
NM_000208.4:c.3035T>A
MANE Select
|
NP_000199.2:p.Val1012Glu
|
|
NM_001079817.3:c.2999T>A
|
NP_001073285.1:p.Val1000Glu
|
|