ENST00000302850.10:c.3057T>G
MANE Select
|
ENSP00000303830.4:p.Ser1019=
|
|
ENST00000302850.9:c.3057T>G
|
ENSP00000303830.4:p.Ser1019=
|
|
ENST00000341500.9:c.3021T>G
|
ENSP00000342838.4:p.Ser1007=
|
|
NM_000208.2:c.3057T>G
|
NP_000199.2:p.Ser1019=
|
|
NM_000208.3:c.3057T>G
|
NP_000199.2:p.Ser1019=
|
|
NM_001079817.1:c.3021T>G
|
NP_001073285.1:p.Ser1007=
|
|
NM_001079817.2:c.3021T>G
|
NP_001073285.1:p.Ser1007=
|
|
XM_011527988.1:c.3132T>G
|
XP_011526290.1:p.Ser1044=
|
|
XM_011527989.1:c.3096T>G
|
XP_011526291.1:p.Ser1032=
|
|
XM_011527988.2:c.3054T>G
|
XP_011526290.2:p.Ser1018=
|
|
XM_011527989.3:c.3018T>G
|
XP_011526291.2:p.Ser1006=
|
|
NM_000208.4:c.3057T>G
MANE Select
|
NP_000199.2:p.Ser1019=
|
|
NM_001079817.3:c.3021T>G
|
NP_001073285.1:p.Ser1007=
|
|