ENST00000557915.2:n.1110G>A
|
|
|
ENST00000557921.3:c.699G>A
|
ENSP00000453157.3:p.Gln233=
|
|
ENST00000699682.1:n.1197G>A
|
|
|
ENST00000699683.1:n.1247G>A
|
|
|
ENST00000699684.1:c.*400G>A
|
ENSP00000514523.1:n.*400G>A
|
|
ENST00000699685.1:n.1011G>A
|
|
|
ENST00000699686.1:c.600G>A
|
ENSP00000514524.1:p.Gln200=
|
|
ENST00000699687.1:c.702G>A
|
ENSP00000514525.1:p.Gln234=
|
|
ENST00000699688.1:n.1007G>A
|
|
|
ENST00000699689.1:n.1363G>A
|
|
|
ENST00000699690.1:n.1560G>A
|
|
|
ENST00000699691.1:n.1704G>A
|
|
|
ENST00000699693.1:n.1224G>A
|
|
|
ENST00000699694.1:n.1466G>A
|
|
|
ENST00000699695.1:c.*179G>A
|
ENSP00000514526.1:n.*179G>A
|
|
ENST00000699696.1:n.1110G>A
|
|
|
ENST00000699697.1:c.807G>A
|
ENSP00000514527.1:p.Gln269=
|
|
ENST00000699698.1:n.728G>A
|
|
|
ENST00000699699.1:n.1131G>A
|
|
|
ENST00000699700.1:n.1254G>A
|
|
|
ENST00000699701.1:c.*187G>A
|
ENSP00000514528.1:n.*187G>A
|
|
ENST00000267415.12:c.807G>A
MANE Select
|
ENSP00000267415.7:p.Gln269=
|
|
ENST00000557921.2:c.699G>A
|
ENSP00000453157.2:p.Gln233=
|
|
ENST00000646753.1:c.702G>A
|
ENSP00000494065.1:p.Gln234=
|
|
ENST00000267415.11:c.807G>A
|
ENSP00000267415.7:p.Gln269=
|
|
ENST00000399423.8:c.807G>A
|
ENSP00000382350.4:p.Gln269=
|
|
ENST00000558476.5:c.369G>A
|
ENSP00000452724.1:p.Gln123=
|
|
ENST00000558566.1:c.*179G>A
|
ENSP00000453025.1:n.*179G>A
|
|
ENST00000559019.1:c.*179G>A
|
ENSP00000453675.1:n.*179G>A
|
|
ENST00000559549.1:n.533G>A
|
|
|
ENST00000559969.5:c.757+6G>A
|
|
|
ENST00000626689.2:c.*179G>A
|
ENSP00000486681.1:n.*179G>A
|
|
NM_001099274.1:c.807G>A
|
NP_001092744.1:p.Gln269=
|
|
NM_012461.2:c.807G>A
|
NP_036593.2:p.Gln269=
|
|
XM_005267528.2:c.807G>A
|
XP_005267585.1:p.Gln269=
|
|
XM_005267529.2:c.702G>A
|
XP_005267586.1:p.Gln234=
|
|
NM_001099274.2:c.807G>A
|
NP_001092744.1:p.Gln269=
|
|
NM_001363668.1:c.702G>A
|
NP_001350597.1:p.Gln234=
|
|
NM_012461.3:c.807G>A
|
NP_036593.2:p.Gln269=
|
|
XM_011536642.2:c.*187G>A
|
XP_011534944.1:n.*187G>A
|
|
XM_017021216.2:c.165G>A
|
XP_016876705.1:p.Gln55=
|
|
XM_017021217.1:c.165G>A
|
XP_016876706.1:p.Gln55=
|
|
NM_001099274.3:c.807G>A
MANE Select
|
NP_001092744.1:p.Gln269=
|
|
NM_001363668.2:c.702G>A
|
NP_001350597.1:p.Gln234=
|
|