ENST00000557915.2:n.1071A>C
|
|
|
ENST00000557921.3:c.660A>C
|
ENSP00000453157.3:p.Arg220=
|
|
ENST00000699682.1:n.1158A>C
|
|
|
ENST00000699683.1:n.1208A>C
|
|
|
ENST00000699684.1:c.*361A>C
|
ENSP00000514523.1:n.*361A>C
|
|
ENST00000699685.1:n.972A>C
|
|
|
ENST00000699686.1:c.561A>C
|
ENSP00000514524.1:p.Arg187=
|
|
ENST00000699687.1:c.663A>C
|
ENSP00000514525.1:p.Arg221=
|
|
ENST00000699688.1:n.968A>C
|
|
|
ENST00000699689.1:n.1324A>C
|
|
|
ENST00000699690.1:n.1521A>C
|
|
|
ENST00000699691.1:n.1665A>C
|
|
|
ENST00000699693.1:n.1185A>C
|
|
|
ENST00000699694.1:n.1427A>C
|
|
|
ENST00000699695.1:c.*140A>C
|
ENSP00000514526.1:n.*140A>C
|
|
ENST00000699696.1:n.1071A>C
|
|
|
ENST00000699697.1:c.768A>C
|
ENSP00000514527.1:p.Arg256=
|
|
ENST00000699698.1:n.689A>C
|
|
|
ENST00000699699.1:n.1092A>C
|
|
|
ENST00000699700.1:n.1215A>C
|
|
|
ENST00000699701.1:c.*148A>C
|
ENSP00000514528.1:n.*148A>C
|
|
ENST00000267415.12:c.768A>C
MANE Select
|
ENSP00000267415.7:p.Arg256=
|
|
ENST00000557921.2:c.660A>C
|
ENSP00000453157.2:p.Arg220=
|
|
ENST00000646753.1:c.663A>C
|
ENSP00000494065.1:p.Arg221=
|
|
ENST00000267415.11:c.768A>C
|
ENSP00000267415.7:p.Arg256=
|
|
ENST00000399423.8:c.768A>C
|
ENSP00000382350.4:p.Arg256=
|
|
ENST00000558476.5:c.330A>C
|
ENSP00000452724.1:p.Arg110=
|
|
ENST00000558566.1:c.*140A>C
|
ENSP00000453025.1:n.*140A>C
|
|
ENST00000559019.1:c.*140A>C
|
ENSP00000453675.1:n.*140A>C
|
|
ENST00000559549.1:n.494A>C
|
|
|
ENST00000559969.5:c.724A>C
|
|
|
ENST00000626689.2:c.*140A>C
|
ENSP00000486681.1:n.*140A>C
|
|
NM_001099274.1:c.768A>C
|
NP_001092744.1:p.Arg256=
|
|
NM_012461.2:c.768A>C
|
NP_036593.2:p.Arg256=
|
|
XM_005267528.2:c.768A>C
|
XP_005267585.1:p.Arg256=
|
|
XM_005267529.2:c.663A>C
|
XP_005267586.1:p.Arg221=
|
|
NM_001099274.2:c.768A>C
|
NP_001092744.1:p.Arg256=
|
|
NM_001363668.1:c.663A>C
|
NP_001350597.1:p.Arg221=
|
|
NM_012461.3:c.768A>C
|
NP_036593.2:p.Arg256=
|
|
XM_011536642.2:c.*148A>C
|
XP_011534944.1:n.*148A>C
|
|
XM_017021216.2:c.126A>C
|
XP_016876705.1:p.Arg42=
|
|
XM_017021217.1:c.126A>C
|
XP_016876706.1:p.Arg42=
|
|
NM_001099274.3:c.768A>C
MANE Select
|
NP_001092744.1:p.Arg256=
|
|
NM_001363668.2:c.663A>C
|
NP_001350597.1:p.Arg221=
|
|