ENST00000557915.2:n.1312G>A
|
|
|
ENST00000557921.3:c.901G>A
|
ENSP00000453157.3:p.Gly301Arg
|
|
ENST00000699682.1:n.1399G>A
|
|
|
ENST00000699683.1:n.1449G>A
|
|
|
ENST00000699684.1:c.*602G>A
|
ENSP00000514523.1:n.*602G>A
|
|
ENST00000699685.1:n.1213G>A
|
|
|
ENST00000699686.1:c.802G>A
|
ENSP00000514524.1:p.Gly268Arg
|
|
ENST00000699687.1:c.904G>A
|
ENSP00000514525.1:p.Gly302Arg
|
|
ENST00000699688.1:n.1209G>A
|
|
|
ENST00000699689.1:n.1565G>A
|
|
|
ENST00000699690.1:n.1762G>A
|
|
|
ENST00000699691.1:n.1906G>A
|
|
|
ENST00000699693.1:n.1426G>A
|
|
|
ENST00000699694.1:n.1668G>A
|
|
|
ENST00000699695.1:c.*381G>A
|
ENSP00000514526.1:n.*381G>A
|
|
ENST00000699696.1:n.1312G>A
|
|
|
ENST00000699697.1:c.1009G>A
|
ENSP00000514527.1:p.Gly337Arg
|
|
ENST00000699698.1:n.930G>A
|
|
|
ENST00000699699.1:n.1333G>A
|
|
|
ENST00000699700.1:n.1456G>A
|
|
|
ENST00000699701.1:c.*389G>A
|
ENSP00000514528.1:n.*389G>A
|
|
ENST00000267415.12:c.1009G>A
MANE Select
|
ENSP00000267415.7:p.Gly337Arg
|
|
ENST00000646753.1:c.904G>A
|
ENSP00000494065.1:p.Gly302Arg
|
|
ENST00000267415.11:c.1009G>A
|
ENSP00000267415.7:p.Gly337Arg
|
|
ENST00000399423.8:c.1009G>A
|
ENSP00000382350.4:p.Gly337Arg
|
|
ENST00000557915.1:n.128G>A
|
|
|
ENST00000558566.1:c.*381G>A
|
ENSP00000453025.1:n.*381G>A
|
|
ENST00000559969.5:c.767G>A
|
|
|
ENST00000560019.5:c.4G>A
|
ENSP00000453113.1:p.Gly2Arg
|
|
ENST00000626689.2:c.*381G>A
|
ENSP00000486681.1:n.*381G>A
|
|
NM_001099274.1:c.1009G>A
|
NP_001092744.1:p.Gly337Arg
|
|
NM_012461.2:c.1009G>A
|
NP_036593.2:p.Gly337Arg
|
|
XM_005267528.2:c.1009G>A
|
XP_005267585.1:p.Gly337Arg
|
|
XM_005267529.2:c.904G>A
|
XP_005267586.1:p.Gly302Arg
|
|
NM_001099274.2:c.1009G>A
|
NP_001092744.1:p.Gly337Arg
|
|
NM_001363668.1:c.904G>A
|
NP_001350597.1:p.Gly302Arg
|
|
NM_012461.3:c.1009G>A
|
NP_036593.2:p.Gly337Arg
|
|
XM_011536642.2:c.*389G>A
|
XP_011534944.1:n.*389G>A
|
|
XM_017021216.2:c.367G>A
|
XP_016876705.1:p.Gly123Arg
|
|
XM_017021217.1:c.367G>A
|
XP_016876706.1:p.Gly123Arg
|
|
NM_001099274.3:c.1009G>A
MANE Select
|
NP_001092744.1:p.Gly337Arg
|
|
NM_001363668.2:c.904G>A
|
NP_001350597.1:p.Gly302Arg
|
|