ENST00000557915.2:n.1216A>C
|
|
|
ENST00000557921.3:c.805A>C
|
ENSP00000453157.3:p.Ser269Arg
|
|
ENST00000699682.1:n.1303A>C
|
|
|
ENST00000699683.1:n.1353A>C
|
|
|
ENST00000699684.1:c.*506A>C
|
ENSP00000514523.1:n.*506A>C
|
|
ENST00000699685.1:n.1117A>C
|
|
|
ENST00000699686.1:c.706A>C
|
ENSP00000514524.1:p.Ser236Arg
|
|
ENST00000699687.1:c.808A>C
|
ENSP00000514525.1:p.Ser270Arg
|
|
ENST00000699688.1:n.1113A>C
|
|
|
ENST00000699689.1:n.1469A>C
|
|
|
ENST00000699690.1:n.1666A>C
|
|
|
ENST00000699691.1:n.1810A>C
|
|
|
ENST00000699693.1:n.1330A>C
|
|
|
ENST00000699694.1:n.1572A>C
|
|
|
ENST00000699695.1:c.*285A>C
|
ENSP00000514526.1:n.*285A>C
|
|
ENST00000699696.1:n.1216A>C
|
|
|
ENST00000699697.1:c.913A>C
|
ENSP00000514527.1:p.Ser305Arg
|
|
ENST00000699698.1:n.834A>C
|
|
|
ENST00000699699.1:n.1237A>C
|
|
|
ENST00000699700.1:n.1360A>C
|
|
|
ENST00000699701.1:c.*293A>C
|
ENSP00000514528.1:n.*293A>C
|
|
ENST00000267415.12:c.913A>C
MANE Select
|
ENSP00000267415.7:p.Ser305Arg
|
|
ENST00000557921.2:c.805A>C
|
ENSP00000453157.2:p.Ser269Arg
|
|
ENST00000646753.1:c.808A>C
|
ENSP00000494065.1:p.Ser270Arg
|
|
ENST00000267415.11:c.913A>C
|
ENSP00000267415.7:p.Ser305Arg
|
|
ENST00000399423.8:c.913A>C
|
ENSP00000382350.4:p.Ser305Arg
|
|
ENST00000557915.1:n.32A>C
|
|
|
ENST00000558566.1:c.*285A>C
|
ENSP00000453025.1:n.*285A>C
|
|
ENST00000559019.1:c.*285A>C
|
ENSP00000453675.1:n.*285A>C
|
|
ENST00000559969.5:c.758-87A>C
|
|
|
ENST00000626689.2:c.*285A>C
|
ENSP00000486681.1:n.*285A>C
|
|
NM_001099274.1:c.913A>C
|
NP_001092744.1:p.Ser305Arg
|
|
NM_012461.2:c.913A>C
|
NP_036593.2:p.Ser305Arg
|
|
XM_005267528.2:c.913A>C
|
XP_005267585.1:p.Ser305Arg
|
|
XM_005267529.2:c.808A>C
|
XP_005267586.1:p.Ser270Arg
|
|
NM_001099274.2:c.913A>C
|
NP_001092744.1:p.Ser305Arg
|
|
NM_001363668.1:c.808A>C
|
NP_001350597.1:p.Ser270Arg
|
|
NM_012461.3:c.913A>C
|
NP_036593.2:p.Ser305Arg
|
|
XM_011536642.2:c.*293A>C
|
XP_011534944.1:n.*293A>C
|
|
XM_017021216.2:c.271A>C
|
XP_016876705.1:p.Ser91Arg
|
|
XM_017021217.1:c.271A>C
|
XP_016876706.1:p.Ser91Arg
|
|
NM_001099274.3:c.913A>C
MANE Select
|
NP_001092744.1:p.Ser305Arg
|
|
NM_001363668.2:c.808A>C
|
NP_001350597.1:p.Ser270Arg
|
|