ENST00000482750.6:c.758-294A>T
|
ENSP00000421262.2:n.758-294A>T
|
|
ENST00000696903.1:n.864A>T
|
|
|
ENST00000374202.7:c.813A>T
MANE Select
|
ENSP00000363318.3:p.Gly271=
|
|
ENST00000642473.1:n.1177A>T
|
|
|
ENST00000644022.1:n.1079A>T
|
|
|
ENST00000644708.1:n.1164-294A>T
|
|
|
ENST00000644911.1:n.1219A>T
|
|
|
ENST00000645266.1:c.813A>T
|
ENSP00000493734.1:p.Gly271=
|
|
ENST00000645518.1:c.813A>T
|
ENSP00000493986.1:p.Gly271=
|
|
ENST00000646106.1:c.813A>T
|
ENSP00000496437.1:p.Gly271=
|
|
ENST00000646505.1:c.813A>T
|
ENSP00000496673.1:p.Gly271=
|
|
ENST00000647492.1:c.813A>T
|
ENSP00000495340.1:p.Gly271=
|
|
ENST00000276110.6:n.1406A>T
|
|
|
ENST00000374188.7:c.42-294A>T
|
ENSP00000363303.3:n.42-294A>T
|
|
ENST00000374202.6:c.813A>T
|
ENSP00000363318.2:p.Gly271=
|
|
ENST00000456850.6:c.243A>T
|
ENSP00000388967.2:p.Gly81=
|
|
ENST00000482750.5:c.171-294A>T
|
|
|
ENST00000512747.3:n.740A>T
|
|
|
NM_000206.2:c.813A>T , LRG_150t1:c.813A>T
|
NP_000197.1:p.Gly271=
|
|
NM_000206.3:c.813A>T
MANE Select
|
NP_000197.1:p.Gly271=
|
|