|
ENST00000432588.6:c.868C>T
|
ENSP00000407473.2:p.Arg290Cys
|
|
|
ENST00000473257.3:c.739C>T
|
ENSP00000501773.1:p.Arg247Cys
|
|
|
ENST00000477812.2:n.1415C>T
|
|
|
|
ENST00000493945.6:c.868C>T
|
ENSP00000494269.1:p.Arg290Cys
|
|
|
ENST00000642480.2:c.868C>T
|
ENSP00000495995.2:p.Arg290Cys
|
|
|
ENST00000645576.1:c.820C>T
|
ENSP00000496101.1:p.Arg274Cys
|
|
|
ENST00000646664.1:c.868C>T
MANE Select
|
ENSP00000494750.1:p.Arg290Cys
|
|
|
ENST00000674681.1:c.868C>T
|
ENSP00000502821.1:p.Arg290Cys
|
|
|
ENST00000675515.1:c.868C>T
|
ENSP00000501862.1:p.Arg290Cys
|
|
|
ENST00000676189.1:c.*411C>T
|
ENSP00000502538.1:n.*411C>T
|
|
|
ENST00000676319.1:c.88-337C>T
|
ENSP00000502193.1:n.88-337C>T
|
|
|
ENST00000676397.1:c.868C>T
|
ENSP00000502286.1:p.Arg290Cys
|
|
|
ENST00000331789.9:c.868C>T
|
ENSP00000349960.4:p.Arg290Cys
|
|
|
ENST00000425660.5:c.*531C>T
|
ENSP00000409264.1:n.*531C>T
|
|
|
ENST00000462494.5:n.1393C>T
|
|
|
|
ENST00000484841.5:n.1023C>T
|
|
|
|
ENST00000493945.5:n.969C>T
|
|
|
|
NM_001101.3:c.868C>T , LRG_132t1:c.868C>T
|
NP_001092.1:p.Arg290Cys
|
|
|
XM_006715764.1:c.502C>T
|
XP_006715827.1:p.Arg168Cys
|
|
|
NM_001101.4:c.868C>T
|
NP_001092.1:p.Arg290Cys
|
|
|
NM_001101.5:c.868C>T
MANE Select
|
NP_001092.1:p.Arg290Cys
|
|
