ENST00000302850.10:c.3859G>A
MANE Select
|
ENSP00000303830.4:p.Val1287Ile
|
|
ENST00000302850.9:c.3859G>A
|
ENSP00000303830.4:p.Val1287Ile
|
|
ENST00000341500.9:c.3823G>A
|
ENSP00000342838.4:p.Val1275Ile
|
|
NM_000208.2:c.3859G>A
|
NP_000199.2:p.Val1287Ile
|
|
NM_000208.3:c.3859G>A
|
NP_000199.2:p.Val1287Ile
|
|
NM_001079817.1:c.3823G>A
|
NP_001073285.1:p.Val1275Ile
|
|
NM_001079817.2:c.3823G>A
|
NP_001073285.1:p.Val1275Ile
|
|
XM_011527988.1:c.3934G>A
|
XP_011526290.1:p.Val1312Ile
|
|
XM_011527989.1:c.3898G>A
|
XP_011526291.1:p.Val1300Ile
|
|
XM_011527988.2:c.3856G>A
|
XP_011526290.2:p.Val1286Ile
|
|
XM_011527989.3:c.3820G>A
|
XP_011526291.2:p.Val1274Ile
|
|
NM_000208.4:c.3859G>A
MANE Select
|
NP_000199.2:p.Val1287Ile
|
|
NM_001079817.3:c.3823G>A
|
NP_001073285.1:p.Val1275Ile
|
|