ENST00000557915.2:n.1520+1G>C
|
|
|
ENST00000557921.3:c.*153G>C
|
ENSP00000453157.3:n.*153G>C
|
|
ENST00000699682.1:n.1608G>C
|
|
|
ENST00000699683.1:n.1658G>C
|
|
|
ENST00000699684.1:c.*811G>C
|
ENSP00000514523.1:n.*811G>C
|
|
ENST00000699685.1:n.1422G>C
|
|
|
ENST00000699686.1:c.*153G>C
|
ENSP00000514524.1:n.*153G>C
|
|
ENST00000699687.1:c.*153G>C
|
ENSP00000514525.1:n.*153G>C
|
|
ENST00000699688.1:n.1418G>C
|
|
|
ENST00000699689.1:n.1774G>C
|
|
|
ENST00000699690.1:n.1971G>C
|
|
|
ENST00000699691.1:n.2115G>C
|
|
|
ENST00000699692.1:n.68+1G>C
|
|
|
ENST00000699693.1:n.1546+1G>C
|
|
|
ENST00000699694.1:n.1877G>C
|
|
|
ENST00000699695.1:c.*501+1G>C
|
ENSP00000514526.1:n.*501+1G>C
|
|
ENST00000699696.1:n.1520+1G>C
|
|
|
ENST00000699697.1:c.1130G>C
|
ENSP00000514527.1:p.Gly377Ala
|
|
ENST00000699698.1:n.1051G>C
|
|
|
ENST00000699699.1:n.1542G>C
|
|
|
ENST00000699700.1:n.1665G>C
|
|
|
ENST00000699701.1:c.*598G>C
|
ENSP00000514528.1:n.*598G>C
|
|
ENST00000267415.12:c.1129+1G>C
MANE Select
|
ENSP00000267415.7:n.1129+1G>C
|
|
ENST00000646753.1:c.1024+1G>C
|
ENSP00000494065.1:n.1024+1G>C
|
|
ENST00000267415.11:c.1129+1G>C
|
ENSP00000267415.7:n.1129+1G>C
|
|
ENST00000399423.8:c.*153G>C
|
ENSP00000382350.4:n.*153G>C
|
|
ENST00000557915.1:n.336+1G>C
|
|
|
ENST00000558566.1:c.*590G>C
|
ENSP00000453025.1:n.*590G>C
|
|
ENST00000559969.5:c.976G>C
|
|
|
ENST00000560019.5:c.124+1G>C
|
ENSP00000453113.1:n.124+1G>C
|
|
ENST00000626689.2:c.*501+1G>C
|
ENSP00000486681.1:n.*501+1G>C
|
|
NM_001099274.1:c.1129+1G>C
|
NP_001092744.1:n.1129+1G>C
|
|
NM_012461.2:c.*153G>C
|
NP_036593.2:n.*153G>C
|
|
XM_005267528.2:c.1129+1G>C
|
XP_005267585.1:n.1129+1G>C
|
|
XM_005267529.2:c.1024+1G>C
|
XP_005267586.1:n.1024+1G>C
|
|
NM_001099274.2:c.1129+1G>C
|
NP_001092744.1:n.1129+1G>C
|
|
NM_001363668.1:c.1024+1G>C
|
NP_001350597.1:n.1024+1G>C
|
|
NM_012461.3:c.*153G>C
|
NP_036593.2:n.*153G>C
|
|
XM_011536642.2:c.*598G>C
|
XP_011534944.1:n.*598G>C
|
|
XM_017021216.2:c.487+1G>C
|
XP_016876705.1:n.487+1G>C
|
|
XM_017021217.1:c.487+1G>C
|
XP_016876706.1:n.487+1G>C
|
|
NM_001099274.3:c.1129+1G>C
MANE Select
|
NP_001092744.1:n.1129+1G>C
|
|
NM_001363668.2:c.1024+1G>C
|
NP_001350597.1:n.1024+1G>C
|
|