ENST00000302850.10:c.3196C>A
MANE Select
|
ENSP00000303830.4:p.Arg1066=
|
|
ENST00000302850.9:c.3196C>A
|
ENSP00000303830.4:p.Arg1066=
|
|
ENST00000341500.9:c.3160C>A
|
ENSP00000342838.4:p.Arg1054=
|
|
ENST00000593970.1:n.42C>A
|
|
|
NM_000208.2:c.3196C>A
|
NP_000199.2:p.Arg1066=
|
|
NM_000208.3:c.3196C>A
|
NP_000199.2:p.Arg1066=
|
|
NM_001079817.1:c.3160C>A
|
NP_001073285.1:p.Arg1054=
|
|
NM_001079817.2:c.3160C>A
|
NP_001073285.1:p.Arg1054=
|
|
XM_011527988.1:c.3271C>A
|
XP_011526290.1:p.Arg1091=
|
|
XM_011527989.1:c.3235C>A
|
XP_011526291.1:p.Arg1079=
|
|
XM_011527988.2:c.3193C>A
|
XP_011526290.2:p.Arg1065=
|
|
XM_011527989.3:c.3157C>A
|
XP_011526291.2:p.Arg1053=
|
|
NM_000208.4:c.3196C>A
MANE Select
|
NP_000199.2:p.Arg1066=
|
|
NM_001079817.3:c.3160C>A
|
NP_001073285.1:p.Arg1054=
|
|