ENST00000681978.1:n.2672T>A
|
|
|
ENST00000682178.1:n.2168T>A
|
|
|
ENST00000682345.1:c.*836T>A
|
ENSP00000508122.1:n.*836T>A
|
|
ENST00000682452.1:n.1467T>A
|
|
|
ENST00000682456.1:c.995T>A
|
ENSP00000508240.1:p.Phe332Tyr
|
|
ENST00000682566.1:n.1919T>A
|
|
|
ENST00000682613.1:n.1448T>A
|
|
|
ENST00000682734.1:c.-38T>A
|
ENSP00000507860.1:n.-38T>A
|
|
ENST00000682820.1:n.1173T>A
|
|
|
ENST00000683004.1:c.*829T>A
|
ENSP00000506936.1:n.*829T>A
|
|
ENST00000683079.1:c.*561T>A
|
ENSP00000507296.1:n.*561T>A
|
|
ENST00000683081.1:c.*973T>A
|
ENSP00000507722.1:n.*973T>A
|
|
ENST00000683181.1:n.415T>A
|
|
|
ENST00000683209.1:n.3462T>A
|
|
|
ENST00000683305.1:c.953T>A
|
ENSP00000508043.1:p.Phe318Tyr
|
|
ENST00000683448.1:c.*56T>A
|
ENSP00000506931.1:n.*56T>A
|
|
ENST00000683478.1:c.*487T>A
|
ENSP00000507793.1:n.*487T>A
|
|
ENST00000683483.1:c.992T>A
|
ENSP00000507719.1:p.Phe331Tyr
|
|
ENST00000683622.1:n.850T>A
|
|
|
ENST00000683751.1:c.641T>A
|
ENSP00000506944.1:p.Phe214Tyr
|
|
ENST00000684036.1:c.953T>A
|
ENSP00000507276.1:p.Phe318Tyr
|
|
ENST00000684129.1:c.-38T>A
|
ENSP00000507174.1:n.-38T>A
|
|
ENST00000684209.1:n.1511T>A
|
|
|
ENST00000684296.1:c.*56T>A
|
ENSP00000507740.1:n.*56T>A
|
|
ENST00000684505.1:c.1085T>A
|
ENSP00000508237.1:p.Phe362Tyr
|
|
ENST00000684552.1:c.*56T>A
|
ENSP00000506899.1:n.*56T>A
|
|
ENST00000684611.1:n.2864T>A
|
|
|
ENST00000684622.1:c.1136T>A
|
ENSP00000507546.1:p.Phe379Tyr
|
|
ENST00000684627.1:c.953T>A
|
ENSP00000507471.1:p.Phe318Tyr
|
|
ENST00000684641.1:c.851T>A
|
ENSP00000507642.1:p.Phe284Tyr
|
|
ENST00000684675.1:c.1177T>A
|
ENSP00000506934.1:p.Phe393Ile
|
|
ENST00000684749.1:n.1205T>A
|
|
|
ENST00000511912.6:c.1136T>A
MANE Select
|
ENSP00000426638.1:p.Phe379Tyr
|
|
ENST00000307738.5:c.995T>A
|
ENSP00000303552.5:p.Phe332Tyr
|
|
ENST00000506422.1:n.106T>A
|
|
|
ENST00000511912.5:c.1136T>A
|
ENSP00000426638.1:p.Phe379Tyr
|
|
NM_001281737.1:c.995T>A
|
NP_001268666.1:p.Phe332Tyr
|
|
NM_001281738.1:c.953T>A
|
NP_001268667.1:p.Phe318Tyr
|
|
NM_004453.3:c.1136T>A
|
NP_004444.2:p.Phe379Tyr
|
|
XM_024453935.1:c.953T>A
|
XP_024309703.1:p.Phe318Tyr
|
|
NM_004453.4:c.1136T>A
MANE Select
|
NP_004444.2:p.Phe379Tyr
|
|
NM_001281737.2:c.995T>A
|
NP_001268666.1:p.Phe332Tyr
|
|