ENST00000557915.2:n.966G>C
|
|
|
ENST00000557921.3:c.555G>C
|
ENSP00000453157.3:p.Gln185His
|
|
ENST00000699682.1:n.1053G>C
|
|
|
ENST00000699683.1:n.1103G>C
|
|
|
ENST00000699684.1:c.*256G>C
|
ENSP00000514523.1:n.*256G>C
|
|
ENST00000699685.1:n.867G>C
|
|
|
ENST00000699686.1:c.456G>C
|
ENSP00000514524.1:p.Gln152His
|
|
ENST00000699687.1:c.558G>C
|
ENSP00000514525.1:p.Gln186His
|
|
ENST00000699688.1:n.863G>C
|
|
|
ENST00000699689.1:n.1219G>C
|
|
|
ENST00000699690.1:n.1416G>C
|
|
|
ENST00000699691.1:n.1560G>C
|
|
|
ENST00000699693.1:n.1080G>C
|
|
|
ENST00000699694.1:n.1322G>C
|
|
|
ENST00000699695.1:c.*35G>C
|
ENSP00000514526.1:n.*35G>C
|
|
ENST00000699696.1:n.966G>C
|
|
|
ENST00000699697.1:c.663G>C
|
ENSP00000514527.1:p.Gln221His
|
|
ENST00000699698.1:n.584G>C
|
|
|
ENST00000699699.1:n.987G>C
|
|
|
ENST00000699700.1:n.1110G>C
|
|
|
ENST00000699701.1:c.*43G>C
|
ENSP00000514528.1:n.*43G>C
|
|
ENST00000267415.12:c.663G>C
MANE Select
|
ENSP00000267415.7:p.Gln221His
|
|
ENST00000557921.2:c.555G>C
|
ENSP00000453157.2:p.Gln185His
|
|
ENST00000646753.1:c.558G>C
|
ENSP00000494065.1:p.Gln186His
|
|
ENST00000267415.11:c.663G>C
|
ENSP00000267415.7:p.Gln221His
|
|
ENST00000399423.8:c.663G>C
|
ENSP00000382350.4:p.Gln221His
|
|
ENST00000558476.5:c.225G>C
|
ENSP00000452724.1:p.Gln75His
|
|
ENST00000558566.1:c.*35G>C
|
ENSP00000453025.1:n.*35G>C
|
|
ENST00000559019.1:c.*35G>C
|
ENSP00000453675.1:n.*35G>C
|
|
ENST00000559549.1:n.389G>C
|
|
|
ENST00000559969.5:c.619G>C
|
|
|
ENST00000626689.2:c.*35G>C
|
ENSP00000486681.1:n.*35G>C
|
|
NM_001099274.1:c.663G>C
|
NP_001092744.1:p.Gln221His
|
|
NM_012461.2:c.663G>C
|
NP_036593.2:p.Gln221His
|
|
XM_005267528.2:c.663G>C
|
XP_005267585.1:p.Gln221His
|
|
XM_005267529.2:c.558G>C
|
XP_005267586.1:p.Gln186His
|
|
XM_011536642.1:c.*43G>C
|
XP_011534944.1:n.*43G>C
|
|
NM_001099274.2:c.663G>C
|
NP_001092744.1:p.Gln221His
|
|
NM_001363668.1:c.558G>C
|
NP_001350597.1:p.Gln186His
|
|
NM_012461.3:c.663G>C
|
NP_036593.2:p.Gln221His
|
|
XM_011536642.2:c.*43G>C
|
XP_011534944.1:n.*43G>C
|
|
XM_017021216.2:c.21G>C
|
XP_016876705.1:p.Gln7His
|
|
XM_017021217.1:c.21G>C
|
XP_016876706.1:p.Gln7His
|
|
NM_001099274.3:c.663G>C
MANE Select
|
NP_001092744.1:p.Gln221His
|
|
NM_001363668.2:c.558G>C
|
NP_001350597.1:p.Gln186His
|
|