ENST00000302850.10:c.3159C>G
MANE Select
|
ENSP00000303830.4:p.Arg1053=
|
|
ENST00000302850.9:c.3159C>G
|
ENSP00000303830.4:p.Arg1053=
|
|
ENST00000341500.9:c.3123C>G
|
ENSP00000342838.4:p.Arg1041=
|
|
ENST00000593970.1:n.5C>G
|
|
|
NM_000208.2:c.3159C>G
|
NP_000199.2:p.Arg1053=
|
|
NM_000208.3:c.3159C>G
|
NP_000199.2:p.Arg1053=
|
|
NM_001079817.1:c.3123C>G
|
NP_001073285.1:p.Arg1041=
|
|
NM_001079817.2:c.3123C>G
|
NP_001073285.1:p.Arg1041=
|
|
XM_011527988.1:c.3234C>G
|
XP_011526290.1:p.Arg1078=
|
|
XM_011527989.1:c.3198C>G
|
XP_011526291.1:p.Arg1066=
|
|
XM_011527988.2:c.3156C>G
|
XP_011526290.2:p.Arg1052=
|
|
XM_011527989.3:c.3120C>G
|
XP_011526291.2:p.Arg1040=
|
|
NM_000208.4:c.3159C>G
MANE Select
|
NP_000199.2:p.Arg1053=
|
|
NM_001079817.3:c.3123C>G
|
NP_001073285.1:p.Arg1041=
|
|