ENST00000302850.10:c.4030G>T
MANE Select
|
ENSP00000303830.4:p.Asp1344Tyr
|
|
ENST00000302850.9:c.4030G>T
|
ENSP00000303830.4:p.Asp1344Tyr
|
|
ENST00000341500.9:c.3994G>T
|
ENSP00000342838.4:p.Asp1332Tyr
|
|
NM_000208.2:c.4030G>T
|
NP_000199.2:p.Asp1344Tyr
|
|
NM_000208.3:c.4030G>T
|
NP_000199.2:p.Asp1344Tyr
|
|
NM_001079817.1:c.3994G>T
|
NP_001073285.1:p.Asp1332Tyr
|
|
NM_001079817.2:c.3994G>T
|
NP_001073285.1:p.Asp1332Tyr
|
|
XM_011527988.1:c.4105G>T
|
XP_011526290.1:p.Asp1369Tyr
|
|
XM_011527989.1:c.4069G>T
|
XP_011526291.1:p.Asp1357Tyr
|
|
XM_011527988.2:c.4027G>T
|
XP_011526290.2:p.Asp1343Tyr
|
|
XM_011527989.3:c.3991G>T
|
XP_011526291.2:p.Asp1331Tyr
|
|
NM_000208.4:c.4030G>T
MANE Select
|
NP_000199.2:p.Asp1344Tyr
|
|
NM_001079817.3:c.3994G>T
|
NP_001073285.1:p.Asp1332Tyr
|
|