ENST00000482750.6:c.758-316T>A
|
ENSP00000421262.2:n.758-316T>A
|
|
ENST00000696903.1:n.842T>A
|
|
|
ENST00000374202.7:c.791T>A
MANE Select
|
ENSP00000363318.3:p.Val264Asp
|
|
ENST00000642473.1:n.1155T>A
|
|
|
ENST00000644022.1:n.1057T>A
|
|
|
ENST00000644708.1:n.1164-316T>A
|
|
|
ENST00000644911.1:n.1197T>A
|
|
|
ENST00000645266.1:c.791T>A
|
ENSP00000493734.1:p.Val264Asp
|
|
ENST00000645518.1:c.791T>A
|
ENSP00000493986.1:p.Val264Asp
|
|
ENST00000646106.1:c.791T>A
|
ENSP00000496437.1:p.Val264Asp
|
|
ENST00000646505.1:c.791T>A
|
ENSP00000496673.1:p.Val264Asp
|
|
ENST00000647492.1:c.791T>A
|
ENSP00000495340.1:p.Val264Asp
|
|
ENST00000276110.6:n.1384T>A
|
|
|
ENST00000374188.7:c.42-316T>A
|
ENSP00000363303.3:n.42-316T>A
|
|
ENST00000374202.6:c.791T>A
|
ENSP00000363318.2:p.Val264Asp
|
|
ENST00000456850.6:c.221T>A
|
ENSP00000388967.2:p.Val74Asp
|
|
ENST00000464642.5:c.659T>A
|
|
|
ENST00000482750.5:c.171-316T>A
|
|
|
ENST00000512747.3:n.718T>A
|
|
|
NM_000206.2:c.791T>A , LRG_150t1:c.791T>A
|
NP_000197.1:p.Val264Asp
|
|
NM_000206.3:c.791T>A
MANE Select
|
NP_000197.1:p.Val264Asp
|
|