ENST00000557915.2:n.1119G>T
|
|
|
ENST00000557921.3:c.708G>T
|
ENSP00000453157.3:p.Trp236Cys
|
|
ENST00000699682.1:n.1206G>T
|
|
|
ENST00000699683.1:n.1256G>T
|
|
|
ENST00000699684.1:c.*409G>T
|
ENSP00000514523.1:n.*409G>T
|
|
ENST00000699685.1:n.1020G>T
|
|
|
ENST00000699686.1:c.609G>T
|
ENSP00000514524.1:p.Trp203Cys
|
|
ENST00000699687.1:c.711G>T
|
ENSP00000514525.1:p.Trp237Cys
|
|
ENST00000699688.1:n.1016G>T
|
|
|
ENST00000699689.1:n.1372G>T
|
|
|
ENST00000699690.1:n.1569G>T
|
|
|
ENST00000699691.1:n.1713G>T
|
|
|
ENST00000699693.1:n.1233G>T
|
|
|
ENST00000699694.1:n.1475G>T
|
|
|
ENST00000699695.1:c.*188G>T
|
ENSP00000514526.1:n.*188G>T
|
|
ENST00000699696.1:n.1119G>T
|
|
|
ENST00000699697.1:c.816G>T
|
ENSP00000514527.1:p.Trp272Cys
|
|
ENST00000699698.1:n.737G>T
|
|
|
ENST00000699699.1:n.1140G>T
|
|
|
ENST00000699700.1:n.1263G>T
|
|
|
ENST00000699701.1:c.*196G>T
|
ENSP00000514528.1:n.*196G>T
|
|
ENST00000267415.12:c.816G>T
MANE Select
|
ENSP00000267415.7:p.Trp272Cys
|
|
ENST00000557921.2:c.708G>T
|
ENSP00000453157.2:p.Trp236Cys
|
|
ENST00000646753.1:c.711G>T
|
ENSP00000494065.1:p.Trp237Cys
|
|
ENST00000267415.11:c.816G>T
|
ENSP00000267415.7:p.Trp272Cys
|
|
ENST00000399423.8:c.816G>T
|
ENSP00000382350.4:p.Trp272Cys
|
|
ENST00000558476.5:c.378G>T
|
ENSP00000452724.1:p.Trp126Cys
|
|
ENST00000558566.1:c.*188G>T
|
ENSP00000453025.1:n.*188G>T
|
|
ENST00000559019.1:c.*188G>T
|
ENSP00000453675.1:n.*188G>T
|
|
ENST00000559549.1:n.542G>T
|
|
|
ENST00000559969.5:c.757+15G>T
|
|
|
ENST00000626689.2:c.*188G>T
|
ENSP00000486681.1:n.*188G>T
|
|
NM_001099274.1:c.816G>T
|
NP_001092744.1:p.Trp272Cys
|
|
NM_012461.2:c.816G>T
|
NP_036593.2:p.Trp272Cys
|
|
XM_005267528.2:c.816G>T
|
XP_005267585.1:p.Trp272Cys
|
|
XM_005267529.2:c.711G>T
|
XP_005267586.1:p.Trp237Cys
|
|
NM_001099274.2:c.816G>T
|
NP_001092744.1:p.Trp272Cys
|
|
NM_001363668.1:c.711G>T
|
NP_001350597.1:p.Trp237Cys
|
|
NM_012461.3:c.816G>T
|
NP_036593.2:p.Trp272Cys
|
|
XM_011536642.2:c.*196G>T
|
XP_011534944.1:n.*196G>T
|
|
XM_017021216.2:c.174G>T
|
XP_016876705.1:p.Trp58Cys
|
|
XM_017021217.1:c.174G>T
|
XP_016876706.1:p.Trp58Cys
|
|
NM_001099274.3:c.816G>T
MANE Select
|
NP_001092744.1:p.Trp272Cys
|
|
NM_001363668.2:c.711G>T
|
NP_001350597.1:p.Trp237Cys
|
|