ENST00000588328.7:c.1395T>C
|
ENSP00000468516.4:p.Phe465=
|
|
ENST00000651901.2:c.1329T>C
|
ENSP00000498922.2:p.Phe443=
|
|
ENST00000698359.1:c.1284T>C
|
ENSP00000513682.1:p.Phe428=
|
|
ENST00000698360.1:c.1380T>C
|
ENSP00000513683.1:p.Phe460=
|
|
ENST00000698361.1:c.1445T>C
|
ENSP00000513684.1:p.Phe482Ser
|
|
ENST00000698362.1:c.*58T>C
|
ENSP00000513685.1:n.*58T>C
|
|
ENST00000698426.1:c.1008T>C
|
ENSP00000513713.1:p.Phe336=
|
|
ENST00000698427.1:c.1371T>C
|
ENSP00000513714.1:p.Phe457=
|
|
ENST00000698428.1:c.1008T>C
|
ENSP00000513715.1:p.Phe336=
|
|
ENST00000698429.1:n.1212T>C
|
|
|
ENST00000698430.1:c.1579T>C
|
|
|
ENST00000698431.1:c.1066T>C
|
ENSP00000513717.1:n.1066T>C
|
|
ENST00000698432.1:c.1138T>C
|
|
|
ENST00000698433.1:n.791T>C
|
|
|
ENST00000244137.12:c.1329T>C
MANE Select
|
ENSP00000244137.5:p.Phe443=
|
|
ENST00000588328.6:c.1384T>C
|
|
|
ENST00000651901.1:c.1325T>C
|
|
|
ENST00000244137.11:c.1329T>C
|
ENSP00000244137.5:p.Phe443=
|
|
ENST00000397032.8:c.1206T>C
|
ENSP00000380226.3:p.Phe402=
|
|
ENST00000436370.7:c.1137T>C
|
ENSP00000391890.2:p.Phe379=
|
|
ENST00000591968.1:n.401T>C
|
|
|
ENST00000593085.1:n.1216T>C
|
|
|
NM_000285.3:c.1329T>C
|
NP_000276.2:p.Phe443=
|
|
NM_001166056.1:c.1206T>C
|
NP_001159528.1:p.Phe402=
|
|
NM_001166057.1:c.1137T>C
|
NP_001159529.1:p.Phe379=
|
|
NM_000285.4:c.1329T>C
MANE Select
|
NP_000276.2:p.Phe443=
|
|
NM_001166056.2:c.1206T>C
|
NP_001159528.1:p.Phe402=
|
|
NM_001166057.2:c.1137T>C
|
NP_001159529.1:p.Phe379=
|
|