ENST00000302850.10:c.3212T>C
MANE Select
|
ENSP00000303830.4:p.Phe1071Ser
|
|
ENST00000302850.9:c.3212T>C
|
ENSP00000303830.4:p.Phe1071Ser
|
|
ENST00000341500.9:c.3176T>C
|
ENSP00000342838.4:p.Phe1059Ser
|
|
ENST00000593970.1:n.58T>C
|
|
|
NM_000208.2:c.3212T>C
|
NP_000199.2:p.Phe1071Ser
|
|
NM_000208.3:c.3212T>C
|
NP_000199.2:p.Phe1071Ser
|
|
NM_001079817.1:c.3176T>C
|
NP_001073285.1:p.Phe1059Ser
|
|
NM_001079817.2:c.3176T>C
|
NP_001073285.1:p.Phe1059Ser
|
|
XM_011527988.1:c.3287T>C
|
XP_011526290.1:p.Phe1096Ser
|
|
XM_011527989.1:c.3251T>C
|
XP_011526291.1:p.Phe1084Ser
|
|
XM_011527988.2:c.3209T>C
|
XP_011526290.2:p.Phe1070Ser
|
|
XM_011527989.3:c.3173T>C
|
XP_011526291.2:p.Phe1058Ser
|
|
NM_000208.4:c.3212T>C
MANE Select
|
NP_000199.2:p.Phe1071Ser
|
|
NM_001079817.3:c.3176T>C
|
NP_001073285.1:p.Phe1059Ser
|
|