ENST00000682424.1:c.1064T>C
|
ENSP00000507321.1:p.Phe355Ser
|
|
ENST00000299427.12:c.1178T>C
MANE Select
|
ENSP00000299427.6:p.Phe393Ser
|
|
ENST00000436873.7:c.415T>C
|
|
|
ENST00000524924.2:n.298T>C
|
|
|
ENST00000533371.6:c.449T>C
|
ENSP00000437066.1:p.Phe150Ser
|
|
ENST00000642892.1:c.449T>C
|
ENSP00000494165.1:p.Phe150Ser
|
|
ENST00000643342.1:c.251T>C
|
|
|
ENST00000643439.1:c.*918T>C
|
ENSP00000495849.1:n.*918T>C
|
|
ENST00000643479.1:n.1364T>C
|
|
|
ENST00000643516.1:c.687T>C
|
|
|
ENST00000644218.1:c.989T>C
|
ENSP00000493574.1:p.Phe330Ser
|
|
ENST00000644683.1:c.*631T>C
|
ENSP00000494085.1:n.*631T>C
|
|
ENST00000644810.1:c.899T>C
|
ENSP00000495895.1:p.Phe300Ser
|
|
ENST00000644831.1:n.1354T>C
|
|
|
ENST00000644933.1:c.*44T>C
|
ENSP00000496133.1:n.*44T>C
|
|
ENST00000645285.1:c.*44T>C
|
ENSP00000495058.1:n.*44T>C
|
|
ENST00000645331.1:n.2383T>C
|
|
|
ENST00000645620.1:c.449T>C
|
ENSP00000493657.1:p.Phe150Ser
|
|
ENST00000646691.1:n.953T>C
|
|
|
ENST00000646777.1:n.1511T>C
|
|
|
ENST00000647016.1:n.1658T>C
|
|
|
ENST00000647152.1:c.449T>C
|
ENSP00000495893.1:p.Phe150Ser
|
|
ENST00000647209.1:c.*1047T>C
|
ENSP00000495558.1:n.*1047T>C
|
|
ENST00000647346.1:n.2198T>C
|
|
|
ENST00000299427.10:c.1178T>C
|
ENSP00000299427.6:p.Phe393Ser
|
|
ENST00000524924.1:n.133T>C
|
|
|
ENST00000532191.1:n.231T>C
|
|
|
ENST00000533371.5:c.449T>C
|
ENSP00000437066.1:p.Phe150Ser
|
|
ENST00000611494.4:c.1178T>C
|
ENSP00000484546.1:p.Phe393Ser
|
|
NM_000391.3:c.1178T>C
|
NP_000382.3:p.Phe393Ser
|
|
NM_000391.4:c.1178T>C
MANE Select
|
NP_000382.3:p.Phe393Ser
|
|