ENST00000302850.10:c.3198A>G
MANE Select
|
ENSP00000303830.4:p.Arg1066=
|
|
ENST00000302850.9:c.3198A>G
|
ENSP00000303830.4:p.Arg1066=
|
|
ENST00000341500.9:c.3162A>G
|
ENSP00000342838.4:p.Arg1054=
|
|
ENST00000593970.1:n.44A>G
|
|
|
NM_000208.2:c.3198A>G
|
NP_000199.2:p.Arg1066=
|
|
NM_000208.3:c.3198A>G
|
NP_000199.2:p.Arg1066=
|
|
NM_001079817.1:c.3162A>G
|
NP_001073285.1:p.Arg1054=
|
|
NM_001079817.2:c.3162A>G
|
NP_001073285.1:p.Arg1054=
|
|
XM_011527988.1:c.3273A>G
|
XP_011526290.1:p.Arg1091=
|
|
XM_011527989.1:c.3237A>G
|
XP_011526291.1:p.Arg1079=
|
|
XM_011527988.2:c.3195A>G
|
XP_011526290.2:p.Arg1065=
|
|
XM_011527989.3:c.3159A>G
|
XP_011526291.2:p.Arg1053=
|
|
NM_000208.4:c.3198A>G
MANE Select
|
NP_000199.2:p.Arg1066=
|
|
NM_001079817.3:c.3162A>G
|
NP_001073285.1:p.Arg1054=
|
|