ENST00000302850.10:c.3893T>C
MANE Select
|
ENSP00000303830.4:p.Phe1298Ser
|
|
ENST00000302850.9:c.3893T>C
|
ENSP00000303830.4:p.Phe1298Ser
|
|
ENST00000341500.9:c.3857T>C
|
ENSP00000342838.4:p.Phe1286Ser
|
|
NM_000208.2:c.3893T>C
|
NP_000199.2:p.Phe1298Ser
|
|
NM_000208.3:c.3893T>C
|
NP_000199.2:p.Phe1298Ser
|
|
NM_001079817.1:c.3857T>C
|
NP_001073285.1:p.Phe1286Ser
|
|
NM_001079817.2:c.3857T>C
|
NP_001073285.1:p.Phe1286Ser
|
|
XM_011527988.1:c.3968T>C
|
XP_011526290.1:p.Phe1323Ser
|
|
XM_011527989.1:c.3932T>C
|
XP_011526291.1:p.Phe1311Ser
|
|
XM_011527988.2:c.3890T>C
|
XP_011526290.2:p.Phe1297Ser
|
|
XM_011527989.3:c.3854T>C
|
XP_011526291.2:p.Phe1285Ser
|
|
NM_000208.4:c.3893T>C
MANE Select
|
NP_000199.2:p.Phe1298Ser
|
|
NM_001079817.3:c.3857T>C
|
NP_001073285.1:p.Phe1286Ser
|
|