ENST00000302850.10:c.3638T>C
MANE Select
|
ENSP00000303830.4:p.Phe1213Ser
|
|
ENST00000302850.9:c.3638T>C
|
ENSP00000303830.4:p.Phe1213Ser
|
|
ENST00000341500.9:c.3602T>C
|
ENSP00000342838.4:p.Phe1201Ser
|
|
ENST00000601099.1:n.549T>C
|
|
|
NM_000208.2:c.3638T>C
|
NP_000199.2:p.Phe1213Ser
|
|
NM_000208.3:c.3638T>C
|
NP_000199.2:p.Phe1213Ser
|
|
NM_001079817.1:c.3602T>C
|
NP_001073285.1:p.Phe1201Ser
|
|
NM_001079817.2:c.3602T>C
|
NP_001073285.1:p.Phe1201Ser
|
|
XM_011527988.1:c.3713T>C
|
XP_011526290.1:p.Phe1238Ser
|
|
XM_011527989.1:c.3677T>C
|
XP_011526291.1:p.Phe1226Ser
|
|
XM_011527988.2:c.3635T>C
|
XP_011526290.2:p.Phe1212Ser
|
|
XM_011527989.3:c.3599T>C
|
XP_011526291.2:p.Phe1200Ser
|
|
NM_000208.4:c.3638T>C
MANE Select
|
NP_000199.2:p.Phe1213Ser
|
|
NM_001079817.3:c.3602T>C
|
NP_001073285.1:p.Phe1201Ser
|
|