ENST00000482750.6:c.399G>T
|
ENSP00000421262.2:p.Gln133His
|
|
ENST00000696903.1:n.450G>T
|
|
|
ENST00000374202.7:c.399G>T
MANE Select
|
ENSP00000363318.3:p.Gln133His
|
|
ENST00000642473.1:n.763G>T
|
|
|
ENST00000644022.1:n.805G>T
|
|
|
ENST00000644708.1:n.805G>T
|
|
|
ENST00000644911.1:n.805G>T
|
|
|
ENST00000645266.1:c.399G>T
|
ENSP00000493734.1:p.Gln133His
|
|
ENST00000645518.1:c.399G>T
|
ENSP00000493986.1:p.Gln133His
|
|
ENST00000646106.1:c.399G>T
|
ENSP00000496437.1:p.Gln133His
|
|
ENST00000646505.1:c.399G>T
|
ENSP00000496673.1:p.Gln133His
|
|
ENST00000647492.1:c.399G>T
|
ENSP00000495340.1:p.Gln133His
|
|
ENST00000276110.6:n.784G>T
|
|
|
ENST00000374188.7:c.-318G>T
|
ENSP00000363303.3:n.-318G>T
|
|
ENST00000374202.6:c.399G>T
|
ENSP00000363318.2:p.Gln133His
|
|
ENST00000456850.6:c.24+866G>T
|
ENSP00000388967.2:n.24+866G>T
|
|
ENST00000464642.5:c.267G>T
|
ENSP00000425233.1:p.Gln89His
|
|
ENST00000487883.1:c.363G>T
|
ENSP00000423966.1:p.Gln121His
|
|
ENST00000512747.3:n.466G>T
|
|
|
NM_000206.2:c.399G>T , LRG_150t1:c.399G>T
|
NP_000197.1:p.Gln133His
|
|
NM_000206.3:c.399G>T
MANE Select
|
NP_000197.1:p.Gln133His
|
|