ENST00000557915.2:n.1517C>G
|
|
|
ENST00000557921.3:c.*149C>G
|
ENSP00000453157.3:n.*149C>G
|
|
ENST00000699682.1:n.1604C>G
|
|
|
ENST00000699683.1:n.1654C>G
|
|
|
ENST00000699684.1:c.*807C>G
|
ENSP00000514523.1:n.*807C>G
|
|
ENST00000699685.1:n.1418C>G
|
|
|
ENST00000699686.1:c.*149C>G
|
ENSP00000514524.1:n.*149C>G
|
|
ENST00000699687.1:c.*149C>G
|
ENSP00000514525.1:n.*149C>G
|
|
ENST00000699688.1:n.1414C>G
|
|
|
ENST00000699689.1:n.1770C>G
|
|
|
ENST00000699690.1:n.1967C>G
|
|
|
ENST00000699691.1:n.2111C>G
|
|
|
ENST00000699692.1:n.65C>G
|
|
|
ENST00000699693.1:n.1543C>G
|
|
|
ENST00000699694.1:n.1873C>G
|
|
|
ENST00000699695.1:c.*498C>G
|
ENSP00000514526.1:n.*498C>G
|
|
ENST00000699696.1:n.1517C>G
|
|
|
ENST00000699697.1:c.1126C>G
|
ENSP00000514527.1:p.Pro376Ala
|
|
ENST00000699698.1:n.1047C>G
|
|
|
ENST00000699699.1:n.1538C>G
|
|
|
ENST00000699700.1:n.1661C>G
|
|
|
ENST00000699701.1:c.*594C>G
|
ENSP00000514528.1:n.*594C>G
|
|
ENST00000267415.12:c.1126C>G
MANE Select
|
ENSP00000267415.7:p.Pro376Ala
|
|
ENST00000646753.1:c.1021C>G
|
ENSP00000494065.1:p.Pro341Ala
|
|
ENST00000267415.11:c.1126C>G
|
ENSP00000267415.7:p.Pro376Ala
|
|
ENST00000399423.8:c.*149C>G
|
ENSP00000382350.4:n.*149C>G
|
|
ENST00000557915.1:n.333C>G
|
|
|
ENST00000558566.1:c.*586C>G
|
ENSP00000453025.1:n.*586C>G
|
|
ENST00000559969.5:c.972C>G
|
|
|
ENST00000560019.5:c.121C>G
|
ENSP00000453113.1:p.Pro41Ala
|
|
ENST00000626689.2:c.*498C>G
|
ENSP00000486681.1:n.*498C>G
|
|
NM_001099274.1:c.1126C>G
|
NP_001092744.1:p.Pro376Ala
|
|
NM_012461.2:c.*149C>G
|
NP_036593.2:n.*149C>G
|
|
XM_005267528.2:c.1126C>G
|
XP_005267585.1:p.Pro376Ala
|
|
XM_005267529.2:c.1021C>G
|
XP_005267586.1:p.Pro341Ala
|
|
NM_001099274.2:c.1126C>G
|
NP_001092744.1:p.Pro376Ala
|
|
NM_001363668.1:c.1021C>G
|
NP_001350597.1:p.Pro341Ala
|
|
NM_012461.3:c.*149C>G
|
NP_036593.2:n.*149C>G
|
|
XM_011536642.2:c.*594C>G
|
XP_011534944.1:n.*594C>G
|
|
XM_017021216.2:c.484C>G
|
XP_016876705.1:p.Pro162Ala
|
|
XM_017021217.1:c.484C>G
|
XP_016876706.1:p.Pro162Ala
|
|
NM_001099274.3:c.1126C>G
MANE Select
|
NP_001092744.1:p.Pro376Ala
|
|
NM_001363668.2:c.1021C>G
|
NP_001350597.1:p.Pro341Ala
|
|