ENST00000285398.7:c.292G>T
MANE Select
|
ENSP00000285398.2:p.Asp98Tyr
|
|
ENST00000642308.1:c.292G>T
|
ENSP00000496684.1:p.Asp98Tyr
|
|
ENST00000644317.1:c.235-85G>T
|
ENSP00000494012.1:n.235-85G>T
|
|
ENST00000645233.1:c.292G>T
|
ENSP00000494116.1:p.Asp98Tyr
|
|
ENST00000645467.1:c.292G>T
|
ENSP00000494889.1:p.Asp98Tyr
|
|
ENST00000645736.1:c.148G>T
|
ENSP00000494545.1:p.Asp50Tyr
|
|
ENST00000646654.1:c.292G>T
|
ENSP00000494526.1:p.Asp98Tyr
|
|
ENST00000647169.1:c.292G>T
|
ENSP00000495619.1:p.Asp98Tyr
|
|
ENST00000285398.6:c.292G>T
|
ENSP00000285398.2:p.Asp98Tyr
|
|
ENST00000426778.5:c.*273G>T
|
ENSP00000415335.1:n.*273G>T
|
|
ENST00000445889.5:c.*335G>T
|
ENSP00000390888.1:n.*335G>T
|
|
ENST00000462306.5:n.291-85G>T
|
|
|
ENST00000490062.1:n.307-85G>T
|
|
|
ENST00000494464.5:n.261-85G>T
|
|
|
NM_000122.1:c.292G>T , LRG_462t1:c.292G>T
|
NP_000113.1:p.Asp98Tyr
|
|
NM_001303416.1:c.100G>T
|
NP_001290345.1:p.Asp34Tyr
|
|
NM_001303418.1:c.100G>T
|
NP_001290347.1:p.Asp34Tyr
|
|
XM_011510794.1:c.292G>T
|
XP_011509096.1:p.Asp98Tyr
|
|
XM_011510795.1:c.-80-85G>T
|
XP_011509097.1:n.-80-85G>T
|
|
XM_011510794.2:c.292G>T
|
XP_011509096.1:p.Asp98Tyr
|
|
XM_017003583.1:c.-80-85G>T
|
XP_016859072.1:n.-80-85G>T
|
|
NM_000122.2:c.292G>T
MANE Select
|
NP_000113.1:p.Asp98Tyr
|
|
NM_001303416.2:c.100G>T
|
NP_001290345.1:p.Asp34Tyr
|
|
NM_001303418.2:c.100G>T
|
NP_001290347.1:p.Asp34Tyr
|
|