|
ENST00000354071.8:n.1077A>T
|
|
|
|
ENST00000461574.2:c.1013A>T
|
ENSP00000417241.2:p.Lys338Ile
|
|
|
ENST00000470026.6:c.1013A>T
|
ENSP00000419274.2:p.Lys338Ile
|
|
|
ENST00000473961.6:c.887A>T
|
ENSP00000420201.2:p.Lys296Ile
|
|
|
ENST00000476777.6:c.1010A>T
|
ENSP00000417554.2:p.Lys337Ile
|
|
|
ENST00000477152.6:c.935A>T
|
ENSP00000419988.2:p.Lys312Ile
|
|
|
ENST00000478531.6:c.784+226A>T
|
ENSP00000420412.2:n.784+226A>T
|
|
|
ENST00000489037.2:c.935A>T
|
ENSP00000420781.2:p.Lys312Ile
|
|
|
ENST00000493919.6:c.646+226A>T
|
ENSP00000418819.2:n.646+226A>T
|
|
|
ENST00000494123.6:c.1013A>T
|
ENSP00000419103.2:p.Lys338Ile
|
|
|
ENST00000497488.2:c.125A>T
|
ENSP00000418986.2:p.Lys42Ile
|
|
|
ENST00000618469.2:c.1013A>T
|
ENSP00000478114.2:p.Lys338Ile
|
|
|
ENST00000634433.2:c.890A>T
|
ENSP00000489431.2:p.Lys297Ile
|
|
|
ENST00000644379.2:c.1013A>T
|
ENSP00000496570.2:p.Lys338Ile
|
|
|
ENST00000644555.2:c.646+226A>T
|
ENSP00000494614.2:n.646+226A>T
|
|
|
ENST00000652672.2:c.872A>T
|
ENSP00000498906.2:p.Lys291Ile
|
|
|
ENST00000484087.6:c.664+226A>T
|
ENSP00000419481.2:n.664+226A>T
|
|
|
ENST00000700182.1:c.706+226A>T
|
ENSP00000514849.1:n.706+226A>T
|
|
|
ENST00000700183.1:c.*1021A>T
|
ENSP00000514850.1:n.*1021A>T
|
|
|
ENST00000357654.9:c.1013A>T
MANE Select
|
ENSP00000350283.3:p.Lys338Ile
|
|
|
ENST00000471181.7:c.1013A>T
|
ENSP00000418960.2:p.Lys338Ile
|
|
|
ENST00000642945.1:c.*887A>T
|
ENSP00000495897.1:n.*887A>T
|
|
|
ENST00000652672.1:c.872A>T
|
ENSP00000498906.1:p.Lys291Ile
|
|
|
ENST00000352993.7:c.670+1328A>T
|
ENSP00000312236.5:n.670+1328A>T
|
|
|
ENST00000354071.7:c.1013A>T
|
ENSP00000326002.7:p.Lys338Ile
|
|
|
ENST00000357654.7:c.1013A>T
|
ENSP00000350283.3:p.Lys338Ile
|
|
|
ENST00000412061.3:c.364A>T
|
|
|
|
ENST00000461221.5:c.*796A>T
|
ENSP00000418548.1:n.*796A>T
|
|
|
ENST00000468300.5:c.787+226A>T
|
ENSP00000417148.1:n.787+226A>T
|
|
|
ENST00000470026.5:c.1013A>T
|
ENSP00000419274.1:p.Lys338Ile
|
|
|
ENST00000471181.6:c.1013A>T
|
ENSP00000418960.2:p.Lys338Ile
|
|
|
ENST00000473961.5:c.610A>T
|
|
|
|
ENST00000477152.5:c.935A>T
|
ENSP00000419988.1:p.Lys312Ile
|
|
|
ENST00000478531.5:c.784+226A>T
|
ENSP00000420412.1:n.784+226A>T
|
|
|
ENST00000484087.5:c.409+226A>T
|
ENSP00000419481.1:n.409+226A>T
|
|
|
ENST00000487825.5:c.412+226A>T
|
ENSP00000418212.1:n.412+226A>T
|
|
|
ENST00000491747.6:c.787+226A>T
|
ENSP00000420705.2:n.787+226A>T
|
|
|
ENST00000492859.5:c.*949A>T
|
ENSP00000420253.1:n.*949A>T
|
|
|
ENST00000493795.5:c.872A>T
|
ENSP00000418775.1:p.Lys291Ile
|
|
|
ENST00000493919.5:c.646+226A>T
|
ENSP00000418819.1:n.646+226A>T
|
|
|
ENST00000494123.5:c.1013A>T
|
ENSP00000419103.1:p.Lys338Ile
|
|
|
ENST00000497488.1:c.125A>T
|
ENSP00000418986.1:p.Lys42Ile
|
|
|
ENST00000586385.5:c.5-30567A>T
|
ENSP00000465818.1:n.5-30567A>T
|
|
|
ENST00000591534.5:c.-43-19997A>T
|
ENSP00000467329.1:n.-43-19997A>T
|
|
|
ENST00000591849.5:c.-99+30753A>T
|
ENSP00000465347.1:n.-99+30753A>T
|
|
|
ENST00000634433.1:c.890A>T
|
ENSP00000489431.1:p.Lys297Ile
|
|
|
NM_007294.3:c.1013A>T , LRG_292t1:c.1013A>T
|
NP_009225.1:p.Lys338Ile
|
|
|
NM_007297.3:c.872A>T
|
NP_009228.2:p.Lys291Ile
|
|
|
NM_007298.3:c.787+226A>T
|
NP_009229.2:n.787+226A>T
|
|
|
NM_007299.3:c.787+226A>T
|
NP_009230.2:n.787+226A>T
|
|
|
NM_007300.3:c.1013A>T
|
NP_009231.2:p.Lys338Ile
|
|
|
NR_027676.1:n.1149A>T
|
|
|
|
NM_007294.4:c.1013A>T
MANE Select
|
NP_009225.1:p.Lys338Ile
|
|
|
NM_007297.4:c.872A>T
|
NP_009228.2:p.Lys291Ile
|
|
|
NM_007299.4:c.787+226A>T
|
NP_009230.2:n.787+226A>T
|
|
|
NM_007300.4:c.1013A>T
|
NP_009231.2:p.Lys338Ile
|
|
|
NR_027676.2:n.1190A>T
|
|
|
