|
ENST00000643817.2:c.337C>T
|
ENSP00000495610.2:p.Arg113Ter
|
|
|
ENST00000686220.1:c.256C>T
|
ENSP00000509904.1:p.Arg86Ter
|
|
|
ENST00000688400.1:c.106-19235C>T
|
ENSP00000510490.1:n.106-19235C>T
|
|
|
ENST00000689156.1:c.337C>T
|
ENSP00000509143.1:p.Arg113Ter
|
|
|
ENST00000691093.1:c.157C>T
|
ENSP00000509465.1:p.Arg53Ter
|
|
|
ENST00000691703.1:c.337C>T
|
ENSP00000508496.1:p.Arg113Ter
|
|
|
ENST00000692664.1:c.187C>T
|
ENSP00000508656.1:p.Arg63Ter
|
|
|
ENST00000693329.1:c.337C>T
|
ENSP00000508490.1:p.Arg113Ter
|
|
|
ENST00000453231.6:c.358C>T
|
ENSP00000392197.2:p.Arg120Ter
|
|
|
ENST00000535845.6:c.256C>T
|
ENSP00000437567.1:p.Arg86Ter
|
|
|
ENST00000538924.7:c.337C>T
MANE Select
|
ENSP00000438346.3:p.Arg113Ter
|
|
|
ENST00000541910.6:c.182+11928C>T
|
ENSP00000442681.1:n.182+11928C>T
|
|
|
ENST00000642243.1:c.295C>T
|
ENSP00000494960.1:p.Arg99Ter
|
|
|
ENST00000643817.1:c.295C>T
|
ENSP00000495610.1:p.Arg99Ter
|
|
|
ENST00000644644.1:c.295C>T
|
ENSP00000494305.1:p.Arg99Ter
|
|
|
ENST00000165698.9:c.337C>T
|
ENSP00000165698.5:p.Arg113Ter
|
|
|
ENST00000428491.5:c.256C>T
|
ENSP00000400607.1:p.Arg86Ter
|
|
|
ENST00000437769.5:c.182+11928C>T
|
ENSP00000401140.1:n.182+11928C>T
|
|
|
ENST00000453231.5:c.358C>T
|
ENSP00000392197.1:p.Arg120Ter
|
|
|
ENST00000473407.5:n.427C>T
|
|
|
|
ENST00000489855.2:c.273C>T
|
|
|
|
ENST00000490915.5:n.359C>T
|
|
|
|
ENST00000535845.5:c.256C>T
|
ENSP00000437567.1:p.Arg86Ter
|
|
|
ENST00000538924.5:c.358C>T
|
ENSP00000438346.1:p.Arg120Ter
|
|
|
ENST00000541910.5:c.182+11928C>T
|
ENSP00000442681.1:n.182+11928C>T
|
|
|
NM_001164730.1:c.358C>T , LRG_713t1:c.358C>T
|
NP_001158202.1:p.Arg120Ter
|
|
|
NM_001164731.1:c.256C>T
|
NP_001158203.1:p.Arg86Ter
|
|
|
NM_001164732.1:c.182+11928C>T
|
NP_001158204.1:n.182+11928C>T
|
|
|
NM_022912.2:c.337C>T , LRG_713t2:c.337C>T
|
NP_075063.1:p.Arg113Ter
|
|
|
XM_005264502.1:c.337C>T
|
XP_005264559.1:p.Arg113Ter
|
|
|
XM_005264504.1:c.223C>T
|
XP_005264561.1:p.Arg75Ter
|
|
|
XM_011533043.1:c.358C>T
|
XP_011531345.1:p.Arg120Ter
|
|
|
XM_011533044.1:c.319C>T
|
XP_011531346.1:p.Arg107Ter
|
|
|
XM_011533045.1:c.313C>T
|
XP_011531347.1:p.Arg105Ter
|
|
|
XM_011533046.1:c.358C>T
|
XP_011531348.1:p.Arg120Ter
|
|
|
XM_005264502.2:c.337C>T
|
XP_005264559.1:p.Arg113Ter
|
|
|
XM_011533045.2:c.313C>T
|
XP_011531347.1:p.Arg105Ter
|
|
|
XM_017004725.1:c.358C>T
|
XP_016860214.1:p.Arg120Ter
|
|
|
XM_017004726.1:c.358C>T
|
XP_016860215.1:p.Arg120Ter
|
|
|
XM_017004727.1:c.358C>T
|
XP_016860216.1:p.Arg120Ter
|
|
|
NM_001164730.2:c.358C>T
|
NP_001158202.1:p.Arg120Ter
|
|
|
NM_001164731.2:c.256C>T
|
NP_001158203.1:p.Arg86Ter
|
|
|
NM_001164732.2:c.182+11928C>T
|
NP_001158204.1:n.182+11928C>T
|
|
|
NM_001371279.1:c.337C>T
MANE Select
|
NP_001358208.1:p.Arg113Ter
|
|
|
NM_001371280.1:c.337C>T
|
NP_001358209.1:p.Arg113Ter
|
|
|
NM_022912.3:c.337C>T
|
NP_075063.1:p.Arg113Ter
|
|
