ENST00000643817.2:c.757A>G
|
ENSP00000495610.2:p.Arg253Gly
|
|
ENST00000686220.1:c.*53A>G
|
ENSP00000509904.1:n.*53A>G
|
|
ENST00000687696.1:n.135A>G
|
|
|
ENST00000687927.1:n.1071A>G
|
|
|
ENST00000688400.1:c.293A>G
|
ENSP00000510490.1:p.Ter98Trp
|
|
ENST00000689156.1:c.427A>G
|
ENSP00000509143.1:p.Arg143Gly
|
|
ENST00000691093.1:c.425A>G
|
ENSP00000509465.1:p.Ter142Trp
|
|
ENST00000691703.1:c.641A>G
|
ENSP00000508496.1:p.Ter214Trp
|
|
ENST00000692664.1:c.455A>G
|
ENSP00000508656.1:p.Ter152Trp
|
|
ENST00000693329.1:c.*79A>G
|
ENSP00000508490.1:n.*79A>G
|
|
ENST00000453231.6:c.626A>G
|
ENSP00000392197.2:p.Ter209Trp
|
|
ENST00000535845.6:c.524A>G
|
ENSP00000437567.1:p.Ter175Trp
|
|
ENST00000538924.7:c.793A>G
MANE Select
|
ENSP00000438346.3:p.Arg265Gly
|
|
ENST00000541910.6:c.370A>G
|
ENSP00000442681.1:p.Arg124Gly
|
|
ENST00000642243.1:c.901A>G
|
ENSP00000494960.1:p.Arg301Gly
|
|
ENST00000643817.1:c.715A>G
|
ENSP00000495610.1:p.Arg239Gly
|
|
ENST00000644644.1:c.802A>G
|
ENSP00000494305.1:p.Arg268Gly
|
|
ENST00000646181.1:n.478A>G
|
|
|
ENST00000165698.9:c.605A>G
|
ENSP00000165698.5:p.Ter202Trp
|
|
ENST00000535845.5:c.524A>G
|
ENSP00000437567.1:p.Ter175Trp
|
|
ENST00000538924.5:c.626A>G
|
ENSP00000438346.1:p.Ter209Trp
|
|
ENST00000541910.5:c.370A>G
|
ENSP00000442681.1:p.Arg124Gly
|
|
NM_001164730.1:c.626A>G , LRG_713t1:c.626A>G
|
NP_001158202.1:p.Ter209Trp
|
|
NM_001164731.1:c.524A>G
|
NP_001158203.1:p.Ter175Trp
|
|
NM_001164732.1:c.370A>G
|
NP_001158204.1:p.Arg124Gly
|
|
NM_022912.2:c.605A>G , LRG_713t2:c.605A>G
|
NP_075063.1:p.Ter202Trp
|
|
XM_005264502.1:c.793A>G
|
XP_005264559.1:p.Arg265Gly
|
|
XM_005264504.1:c.679A>G
|
XP_005264561.1:p.Arg227Gly
|
|
XM_011533043.1:c.778A>G
|
XP_011531345.1:p.Arg260Gly
|
|
XM_011533044.1:c.775A>G
|
XP_011531346.1:p.Arg259Gly
|
|
XM_011533045.1:c.769A>G
|
XP_011531347.1:p.Arg257Gly
|
|
XM_011533046.1:c.662A>G
|
XP_011531348.1:p.Ter221Trp
|
|
XM_005264502.2:c.793A>G
|
XP_005264559.1:p.Arg265Gly
|
|
XM_011533045.2:c.769A>G
|
XP_011531347.1:p.Arg257Gly
|
|
XM_017004725.1:c.778A>G
|
XP_016860214.1:p.Arg260Gly
|
|
XM_017004726.1:c.662A>G
|
XP_016860215.1:p.Ter221Trp
|
|
XM_017004727.1:c.626A>G
|
XP_016860216.1:p.Ter209Trp
|
|
NM_001164730.2:c.626A>G
|
NP_001158202.1:p.Ter209Trp
|
|
NM_001164731.2:c.524A>G
|
NP_001158203.1:p.Ter175Trp
|
|
NM_001164732.2:c.370A>G
|
NP_001158204.1:p.Arg124Gly
|
|
NM_001371279.1:c.793A>G
MANE Select
|
NP_001358208.1:p.Arg265Gly
|
|
NM_001371280.1:c.427A>G
|
NP_001358209.1:p.Arg143Gly
|
|
NM_022912.3:c.605A>G
|
NP_075063.1:p.Ter202Trp
|
|