ENST00000557915.2:n.1133G>T
|
|
|
ENST00000557921.3:c.722G>T
|
ENSP00000453157.3:p.Gly241Val
|
|
ENST00000699682.1:n.1220G>T
|
|
|
ENST00000699683.1:n.1270G>T
|
|
|
ENST00000699684.1:c.*423G>T
|
ENSP00000514523.1:n.*423G>T
|
|
ENST00000699685.1:n.1034G>T
|
|
|
ENST00000699686.1:c.623G>T
|
ENSP00000514524.1:p.Gly208Val
|
|
ENST00000699687.1:c.725G>T
|
ENSP00000514525.1:p.Gly242Val
|
|
ENST00000699688.1:n.1030G>T
|
|
|
ENST00000699689.1:n.1386G>T
|
|
|
ENST00000699690.1:n.1583G>T
|
|
|
ENST00000699691.1:n.1727G>T
|
|
|
ENST00000699693.1:n.1247G>T
|
|
|
ENST00000699694.1:n.1489G>T
|
|
|
ENST00000699695.1:c.*202G>T
|
ENSP00000514526.1:n.*202G>T
|
|
ENST00000699696.1:n.1133G>T
|
|
|
ENST00000699697.1:c.830G>T
|
ENSP00000514527.1:p.Gly277Val
|
|
ENST00000699698.1:n.751G>T
|
|
|
ENST00000699699.1:n.1154G>T
|
|
|
ENST00000699700.1:n.1277G>T
|
|
|
ENST00000699701.1:c.*210G>T
|
ENSP00000514528.1:n.*210G>T
|
|
ENST00000267415.12:c.830G>T
MANE Select
|
ENSP00000267415.7:p.Gly277Val
|
|
ENST00000557921.2:c.722G>T
|
ENSP00000453157.2:p.Gly241Val
|
|
ENST00000646753.1:c.725G>T
|
ENSP00000494065.1:p.Gly242Val
|
|
ENST00000267415.11:c.830G>T
|
ENSP00000267415.7:p.Gly277Val
|
|
ENST00000399423.8:c.830G>T
|
ENSP00000382350.4:p.Gly277Val
|
|
ENST00000558476.5:c.392G>T
|
ENSP00000452724.1:p.Gly131Val
|
|
ENST00000558566.1:c.*202G>T
|
ENSP00000453025.1:n.*202G>T
|
|
ENST00000559019.1:c.*202G>T
|
ENSP00000453675.1:n.*202G>T
|
|
ENST00000559549.1:n.556G>T
|
|
|
ENST00000559969.5:c.757+29G>T
|
|
|
ENST00000626689.2:c.*202G>T
|
ENSP00000486681.1:n.*202G>T
|
|
NM_001099274.1:c.830G>T
|
NP_001092744.1:p.Gly277Val
|
|
NM_012461.2:c.830G>T
|
NP_036593.2:p.Gly277Val
|
|
XM_005267528.2:c.830G>T
|
XP_005267585.1:p.Gly277Val
|
|
XM_005267529.2:c.725G>T
|
XP_005267586.1:p.Gly242Val
|
|
NM_001099274.2:c.830G>T
|
NP_001092744.1:p.Gly277Val
|
|
NM_001363668.1:c.725G>T
|
NP_001350597.1:p.Gly242Val
|
|
NM_012461.3:c.830G>T
|
NP_036593.2:p.Gly277Val
|
|
XM_011536642.2:c.*210G>T
|
XP_011534944.1:n.*210G>T
|
|
XM_017021216.2:c.188G>T
|
XP_016876705.1:p.Gly63Val
|
|
XM_017021217.1:c.188G>T
|
XP_016876706.1:p.Gly63Val
|
|
NM_001099274.3:c.830G>T
MANE Select
|
NP_001092744.1:p.Gly277Val
|
|
NM_001363668.2:c.725G>T
|
NP_001350597.1:p.Gly242Val
|
|