ENST00000482750.6:c.*33G>T
|
ENSP00000421262.2:n.*33G>T
|
|
ENST00000696903.1:n.1216G>T
|
|
|
ENST00000374202.7:c.913G>T
MANE Select
|
ENSP00000363318.3:p.Gly305Trp
|
|
ENST00000642473.1:n.1277G>T
|
|
|
ENST00000644022.1:n.1179G>T
|
|
|
ENST00000644708.1:n.1222G>T
|
|
|
ENST00000644911.1:n.1319G>T
|
|
|
ENST00000645266.1:c.913G>T
|
ENSP00000493734.1:p.Gly305Trp
|
|
ENST00000645518.1:c.913G>T
|
ENSP00000493986.1:p.Gly305Trp
|
|
ENST00000646106.1:c.913G>T
|
ENSP00000496437.1:p.Gly305Trp
|
|
ENST00000646505.1:c.913G>T
|
ENSP00000496673.1:p.Gly305Trp
|
|
ENST00000647492.1:c.913G>T
|
ENSP00000495340.1:p.Gly305Trp
|
|
ENST00000276110.6:n.1506G>T
|
|
|
ENST00000374188.7:c.100G>T
|
ENSP00000363303.3:p.Gly34Trp
|
|
ENST00000374202.6:c.913G>T
|
ENSP00000363318.2:p.Gly305Trp
|
|
ENST00000456850.6:c.343G>T
|
ENSP00000388967.2:p.Gly115Trp
|
|
ENST00000482750.5:c.229G>T
|
|
|
ENST00000512747.3:n.1092G>T
|
|
|
NM_000206.2:c.913G>T , LRG_150t1:c.913G>T
|
NP_000197.1:p.Gly305Trp
|
|
NM_000206.3:c.913G>T
MANE Select
|
NP_000197.1:p.Gly305Trp
|
|