ENST00000557915.2:n.1393G>A
|
|
|
ENST00000557921.3:c.*25G>A
|
ENSP00000453157.3:n.*25G>A
|
|
ENST00000699682.1:n.1480G>A
|
|
|
ENST00000699683.1:n.1530G>A
|
|
|
ENST00000699684.1:c.*683G>A
|
ENSP00000514523.1:n.*683G>A
|
|
ENST00000699685.1:n.1294G>A
|
|
|
ENST00000699686.1:c.*25G>A
|
ENSP00000514524.1:n.*25G>A
|
|
ENST00000699687.1:c.*25G>A
|
ENSP00000514525.1:n.*25G>A
|
|
ENST00000699688.1:n.1290G>A
|
|
|
ENST00000699689.1:n.1646G>A
|
|
|
ENST00000699690.1:n.1843G>A
|
|
|
ENST00000699691.1:n.1987G>A
|
|
|
ENST00000699693.1:n.1478+29G>A
|
|
|
ENST00000699694.1:n.1749G>A
|
|
|
ENST00000699695.1:c.*433+29G>A
|
ENSP00000514526.1:n.*433+29G>A
|
|
ENST00000699696.1:n.1393G>A
|
|
|
ENST00000699697.1:c.1061+29G>A
|
ENSP00000514527.1:n.1061+29G>A
|
|
ENST00000699698.1:n.982+29G>A
|
|
|
ENST00000699699.1:n.1414G>A
|
|
|
ENST00000699700.1:n.1537G>A
|
|
|
ENST00000699701.1:c.*470G>A
|
ENSP00000514528.1:n.*470G>A
|
|
ENST00000267415.12:c.1061+29G>A
MANE Select
|
ENSP00000267415.7:n.1061+29G>A
|
|
ENST00000646753.1:c.956+29G>A
|
ENSP00000494065.1:n.956+29G>A
|
|
ENST00000267415.11:c.1061+29G>A
|
ENSP00000267415.7:n.1061+29G>A
|
|
ENST00000399423.8:c.*25G>A
|
ENSP00000382350.4:n.*25G>A
|
|
ENST00000557915.1:n.209G>A
|
|
|
ENST00000558566.1:c.*462G>A
|
ENSP00000453025.1:n.*462G>A
|
|
ENST00000559969.5:c.848G>A
|
|
|
ENST00000560019.5:c.56+29G>A
|
ENSP00000453113.1:n.56+29G>A
|
|
ENST00000626689.2:c.*433+29G>A
|
ENSP00000486681.1:n.*433+29G>A
|
|
NM_001099274.1:c.1061+29G>A
|
NP_001092744.1:n.1061+29G>A
|
|
NM_012461.2:c.*25G>A
|
NP_036593.2:n.*25G>A
|
|
XM_005267528.2:c.1061+29G>A
|
XP_005267585.1:n.1061+29G>A
|
|
XM_005267529.2:c.956+29G>A
|
XP_005267586.1:n.956+29G>A
|
|
NM_001099274.2:c.1061+29G>A
|
NP_001092744.1:n.1061+29G>A
|
|
NM_001363668.1:c.956+29G>A
|
NP_001350597.1:n.956+29G>A
|
|
NM_012461.3:c.*25G>A
|
NP_036593.2:n.*25G>A
|
|
XM_011536642.2:c.*470G>A
|
XP_011534944.1:n.*470G>A
|
|
XM_017021216.2:c.419+29G>A
|
XP_016876705.1:n.419+29G>A
|
|
XM_017021217.1:c.419+29G>A
|
XP_016876706.1:n.419+29G>A
|
|
NM_001099274.3:c.1061+29G>A
MANE Select
|
NP_001092744.1:n.1061+29G>A
|
|
NM_001363668.2:c.956+29G>A
|
NP_001350597.1:n.956+29G>A
|
|