ENST00000461574.2:c.4622C>T
|
ENSP00000417241.2:p.Ser1541Phe
|
|
ENST00000470026.6:c.4625C>T
|
ENSP00000419274.2:p.Ser1542Phe
|
|
ENST00000473961.6:c.4499C>T
|
ENSP00000420201.2:p.Ser1500Phe
|
|
ENST00000476777.6:c.4619C>T
|
ENSP00000417554.2:p.Ser1540Phe
|
|
ENST00000477152.6:c.4547C>T
|
ENSP00000419988.2:p.Ser1516Phe
|
|
ENST00000478531.6:c.1313C>T
|
ENSP00000420412.2:p.Ser438Phe
|
|
ENST00000489037.2:c.4547C>T
|
ENSP00000420781.2:p.Ser1516Phe
|
|
ENST00000493919.6:c.1175C>T
|
ENSP00000418819.2:p.Ser392Phe
|
|
ENST00000494123.6:c.4625C>T
|
ENSP00000419103.2:p.Ser1542Phe
|
|
ENST00000497488.2:c.3737C>T
|
ENSP00000418986.2:p.Ser1246Phe
|
|
ENST00000618469.2:c.4625C>T
|
ENSP00000478114.2:p.Ser1542Phe
|
|
ENST00000634433.2:c.4502C>T
|
ENSP00000489431.2:p.Ser1501Phe
|
|
ENST00000644379.2:c.4691C>T
|
ENSP00000496570.2:p.Ser1564Phe
|
|
ENST00000644555.2:c.1175C>T
|
ENSP00000494614.2:p.Ser392Phe
|
|
ENST00000652672.2:c.4484C>T
|
ENSP00000498906.2:p.Ser1495Phe
|
|
ENST00000484087.6:c.1187C>T
|
ENSP00000419481.2:p.Ser396Phe
|
|
ENST00000700182.1:c.1232C>T
|
ENSP00000514849.1:p.Ser411Phe
|
|
ENST00000357654.9:c.4625C>T
MANE Select
|
ENSP00000350283.3:p.Ser1542Phe
|
|
ENST00000471181.7:c.4688C>T
|
ENSP00000418960.2:p.Ser1563Phe
|
|
ENST00000644379.1:c.1012C>T
|
|
|
ENST00000352993.7:c.1199C>T
|
ENSP00000312236.5:p.Ser400Phe
|
|
ENST00000357654.7:c.4625C>T
|
ENSP00000350283.3:p.Ser1542Phe
|
|
ENST00000461221.5:c.*4408C>T
|
ENSP00000418548.1:n.*4408C>T
|
|
ENST00000468300.5:c.1313C>T
|
ENSP00000417148.1:p.Ser438Phe
|
|
ENST00000471181.6:c.4688C>T
|
ENSP00000418960.2:p.Ser1563Phe
|
|
ENST00000478531.5:c.1313C>T
|
ENSP00000420412.1:p.Ser438Phe
|
|
ENST00000484087.5:c.938C>T
|
ENSP00000419481.1:p.Ser313Phe
|
|
ENST00000491747.6:c.1313C>T
|
ENSP00000420705.2:p.Ser438Phe
|
|
ENST00000493795.5:c.4484C>T
|
ENSP00000418775.1:p.Ser1495Phe
|
|
ENST00000493919.5:c.1175C>T
|
ENSP00000418819.1:p.Ser392Phe
|
|
ENST00000586385.5:c.5-10430C>T
|
ENSP00000465818.1:n.5-10430C>T
|
|
ENST00000591534.5:c.98C>T
|
ENSP00000467329.1:p.Ser33Phe
|
|
ENST00000591849.5:c.-98-24191C>T
|
ENSP00000465347.1:n.-98-24191C>T
|
|
NM_007294.3:c.4625C>T , LRG_292t1:c.4625C>T
|
NP_009225.1:p.Ser1542Phe
|
|
NM_007297.3:c.4484C>T
|
NP_009228.2:p.Ser1495Phe
|
|
NM_007298.3:c.1313C>T
|
NP_009229.2:p.Ser438Phe
|
|
NM_007299.3:c.1313C>T
|
NP_009230.2:p.Ser438Phe
|
|
NM_007300.3:c.4688C>T
|
NP_009231.2:p.Ser1563Phe
|
|
NR_027676.1:n.4761C>T
|
|
|
NM_007294.4:c.4625C>T
MANE Select
|
NP_009225.1:p.Ser1542Phe
|
|
NM_007297.4:c.4484C>T
|
NP_009228.2:p.Ser1495Phe
|
|
NM_007299.4:c.1313C>T
|
NP_009230.2:p.Ser438Phe
|
|
NM_007300.4:c.4688C>T
|
NP_009231.2:p.Ser1563Phe
|
|
NR_027676.2:n.4802C>T
|
|
|