ENST00000557915.2:n.1149C>T
|
|
|
ENST00000557921.3:c.738C>T
|
ENSP00000453157.3:p.Arg246=
|
|
ENST00000699682.1:n.1236C>T
|
|
|
ENST00000699683.1:n.1286C>T
|
|
|
ENST00000699684.1:c.*439C>T
|
ENSP00000514523.1:n.*439C>T
|
|
ENST00000699685.1:n.1050C>T
|
|
|
ENST00000699686.1:c.639C>T
|
ENSP00000514524.1:p.Arg213=
|
|
ENST00000699687.1:c.741C>T
|
ENSP00000514525.1:p.Arg247=
|
|
ENST00000699688.1:n.1046C>T
|
|
|
ENST00000699689.1:n.1402C>T
|
|
|
ENST00000699690.1:n.1599C>T
|
|
|
ENST00000699691.1:n.1743C>T
|
|
|
ENST00000699693.1:n.1263C>T
|
|
|
ENST00000699694.1:n.1505C>T
|
|
|
ENST00000699695.1:c.*218C>T
|
ENSP00000514526.1:n.*218C>T
|
|
ENST00000699696.1:n.1149C>T
|
|
|
ENST00000699697.1:c.846C>T
|
ENSP00000514527.1:p.Arg282=
|
|
ENST00000699698.1:n.767C>T
|
|
|
ENST00000699699.1:n.1170C>T
|
|
|
ENST00000699700.1:n.1293C>T
|
|
|
ENST00000699701.1:c.*226C>T
|
ENSP00000514528.1:n.*226C>T
|
|
ENST00000267415.12:c.846C>T
MANE Select
|
ENSP00000267415.7:p.Arg282=
|
|
ENST00000557921.2:c.738C>T
|
ENSP00000453157.2:p.Arg246=
|
|
ENST00000646753.1:c.741C>T
|
ENSP00000494065.1:p.Arg247=
|
|
ENST00000267415.11:c.846C>T
|
ENSP00000267415.7:p.Arg282=
|
|
ENST00000399423.8:c.846C>T
|
ENSP00000382350.4:p.Arg282=
|
|
ENST00000558476.5:c.408C>T
|
ENSP00000452724.1:p.Arg136=
|
|
ENST00000558566.1:c.*218C>T
|
ENSP00000453025.1:n.*218C>T
|
|
ENST00000559019.1:c.*218C>T
|
ENSP00000453675.1:n.*218C>T
|
|
ENST00000559549.1:n.572C>T
|
|
|
ENST00000559969.5:c.757+45C>T
|
|
|
ENST00000626689.2:c.*218C>T
|
ENSP00000486681.1:n.*218C>T
|
|
NM_001099274.1:c.846C>T
|
NP_001092744.1:p.Arg282=
|
|
NM_012461.2:c.846C>T
|
NP_036593.2:p.Arg282=
|
|
XM_005267528.2:c.846C>T
|
XP_005267585.1:p.Arg282=
|
|
XM_005267529.2:c.741C>T
|
XP_005267586.1:p.Arg247=
|
|
NM_001099274.2:c.846C>T
|
NP_001092744.1:p.Arg282=
|
|
NM_001363668.1:c.741C>T
|
NP_001350597.1:p.Arg247=
|
|
NM_012461.3:c.846C>T
|
NP_036593.2:p.Arg282=
|
|
XM_011536642.2:c.*226C>T
|
XP_011534944.1:n.*226C>T
|
|
XM_017021216.2:c.204C>T
|
XP_016876705.1:p.Arg68=
|
|
XM_017021217.1:c.204C>T
|
XP_016876706.1:p.Arg68=
|
|
NM_001099274.3:c.846C>T
MANE Select
|
NP_001092744.1:p.Arg282=
|
|
NM_001363668.2:c.741C>T
|
NP_001350597.1:p.Arg247=
|
|