ENST00000302850.10:c.3114T>C
MANE Select
|
ENSP00000303830.4:p.Tyr1038=
|
|
ENST00000302850.9:c.3114T>C
|
ENSP00000303830.4:p.Tyr1038=
|
|
ENST00000341500.9:c.3078T>C
|
ENSP00000342838.4:p.Tyr1026=
|
|
NM_000208.2:c.3114T>C
|
NP_000199.2:p.Tyr1038=
|
|
NM_000208.3:c.3114T>C
|
NP_000199.2:p.Tyr1038=
|
|
NM_001079817.1:c.3078T>C
|
NP_001073285.1:p.Tyr1026=
|
|
NM_001079817.2:c.3078T>C
|
NP_001073285.1:p.Tyr1026=
|
|
XM_011527988.1:c.3189T>C
|
XP_011526290.1:p.Tyr1063=
|
|
XM_011527989.1:c.3153T>C
|
XP_011526291.1:p.Tyr1051=
|
|
XM_011527988.2:c.3111T>C
|
XP_011526290.2:p.Tyr1037=
|
|
XM_011527989.3:c.3075T>C
|
XP_011526291.2:p.Tyr1025=
|
|
NM_000208.4:c.3114T>C
MANE Select
|
NP_000199.2:p.Tyr1038=
|
|
NM_001079817.3:c.3078T>C
|
NP_001073285.1:p.Tyr1026=
|
|