ENST00000302850.10:c.4051T>A
MANE Select
|
ENSP00000303830.4:p.Phe1351Ile
|
|
ENST00000302850.9:c.4051T>A
|
ENSP00000303830.4:p.Phe1351Ile
|
|
ENST00000341500.9:c.4015T>A
|
ENSP00000342838.4:p.Phe1339Ile
|
|
NM_000208.2:c.4051T>A
|
NP_000199.2:p.Phe1351Ile
|
|
NM_000208.3:c.4051T>A
|
NP_000199.2:p.Phe1351Ile
|
|
NM_001079817.1:c.4015T>A
|
NP_001073285.1:p.Phe1339Ile
|
|
NM_001079817.2:c.4015T>A
|
NP_001073285.1:p.Phe1339Ile
|
|
XM_011527988.1:c.4126T>A
|
XP_011526290.1:p.Phe1376Ile
|
|
XM_011527989.1:c.4090T>A
|
XP_011526291.1:p.Phe1364Ile
|
|
XM_011527988.2:c.4048T>A
|
XP_011526290.2:p.Phe1350Ile
|
|
XM_011527989.3:c.4012T>A
|
XP_011526291.2:p.Phe1338Ile
|
|
NM_000208.4:c.4051T>A
MANE Select
|
NP_000199.2:p.Phe1351Ile
|
|
NM_001079817.3:c.4015T>A
|
NP_001073285.1:p.Phe1339Ile
|
|