ENST00000302850.10:c.3665T>C
MANE Select
|
ENSP00000303830.4:p.Phe1222Ser
|
|
ENST00000302850.9:c.3665T>C
|
ENSP00000303830.4:p.Phe1222Ser
|
|
ENST00000341500.9:c.3629T>C
|
ENSP00000342838.4:p.Phe1210Ser
|
|
NM_000208.2:c.3665T>C
|
NP_000199.2:p.Phe1222Ser
|
|
NM_000208.3:c.3665T>C
|
NP_000199.2:p.Phe1222Ser
|
|
NM_001079817.1:c.3629T>C
|
NP_001073285.1:p.Phe1210Ser
|
|
NM_001079817.2:c.3629T>C
|
NP_001073285.1:p.Phe1210Ser
|
|
XM_011527988.1:c.3740T>C
|
XP_011526290.1:p.Phe1247Ser
|
|
XM_011527989.1:c.3704T>C
|
XP_011526291.1:p.Phe1235Ser
|
|
XM_011527988.2:c.3662T>C
|
XP_011526290.2:p.Phe1221Ser
|
|
XM_011527989.3:c.3626T>C
|
XP_011526291.2:p.Phe1209Ser
|
|
NM_000208.4:c.3665T>C
MANE Select
|
NP_000199.2:p.Phe1222Ser
|
|
NM_001079817.3:c.3629T>C
|
NP_001073285.1:p.Phe1210Ser
|
|