ENST00000302850.10:c.3663C>G
MANE Select
|
ENSP00000303830.4:p.Ser1221=
|
|
ENST00000302850.9:c.3663C>G
|
ENSP00000303830.4:p.Ser1221=
|
|
ENST00000341500.9:c.3627C>G
|
ENSP00000342838.4:p.Ser1209=
|
|
NM_000208.2:c.3663C>G
|
NP_000199.2:p.Ser1221=
|
|
NM_000208.3:c.3663C>G
|
NP_000199.2:p.Ser1221=
|
|
NM_001079817.1:c.3627C>G
|
NP_001073285.1:p.Ser1209=
|
|
NM_001079817.2:c.3627C>G
|
NP_001073285.1:p.Ser1209=
|
|
XM_011527988.1:c.3738C>G
|
XP_011526290.1:p.Ser1246=
|
|
XM_011527989.1:c.3702C>G
|
XP_011526291.1:p.Ser1234=
|
|
XM_011527988.2:c.3660C>G
|
XP_011526290.2:p.Ser1220=
|
|
XM_011527989.3:c.3624C>G
|
XP_011526291.2:p.Ser1208=
|
|
NM_000208.4:c.3663C>G
MANE Select
|
NP_000199.2:p.Ser1221=
|
|
NM_001079817.3:c.3627C>G
|
NP_001073285.1:p.Ser1209=
|
|