ENST00000302850.10:c.3213C>T
MANE Select
|
ENSP00000303830.4:p.Phe1071=
|
|
ENST00000302850.9:c.3213C>T
|
ENSP00000303830.4:p.Phe1071=
|
|
ENST00000341500.9:c.3177C>T
|
ENSP00000342838.4:p.Phe1059=
|
|
ENST00000593970.1:n.59C>T
|
|
|
NM_000208.2:c.3213C>T
|
NP_000199.2:p.Phe1071=
|
|
NM_000208.3:c.3213C>T
|
NP_000199.2:p.Phe1071=
|
|
NM_001079817.1:c.3177C>T
|
NP_001073285.1:p.Phe1059=
|
|
NM_001079817.2:c.3177C>T
|
NP_001073285.1:p.Phe1059=
|
|
XM_011527988.1:c.3288C>T
|
XP_011526290.1:p.Phe1096=
|
|
XM_011527989.1:c.3252C>T
|
XP_011526291.1:p.Phe1084=
|
|
XM_011527988.2:c.3210C>T
|
XP_011526290.2:p.Phe1070=
|
|
XM_011527989.3:c.3174C>T
|
XP_011526291.2:p.Phe1058=
|
|
NM_000208.4:c.3213C>T
MANE Select
|
NP_000199.2:p.Phe1071=
|
|
NM_001079817.3:c.3177C>T
|
NP_001073285.1:p.Phe1059=
|
|