ENST00000482750.6:c.758-295G>C
|
ENSP00000421262.2:n.758-295G>C
|
|
ENST00000696903.1:n.863G>C
|
|
|
ENST00000374202.7:c.812G>C
MANE Select
|
ENSP00000363318.3:p.Gly271Ala
|
|
ENST00000642473.1:n.1176G>C
|
|
|
ENST00000644022.1:n.1078G>C
|
|
|
ENST00000644708.1:n.1164-295G>C
|
|
|
ENST00000644911.1:n.1218G>C
|
|
|
ENST00000645266.1:c.812G>C
|
ENSP00000493734.1:p.Gly271Ala
|
|
ENST00000645518.1:c.812G>C
|
ENSP00000493986.1:p.Gly271Ala
|
|
ENST00000646106.1:c.812G>C
|
ENSP00000496437.1:p.Gly271Ala
|
|
ENST00000646505.1:c.812G>C
|
ENSP00000496673.1:p.Gly271Ala
|
|
ENST00000647492.1:c.812G>C
|
ENSP00000495340.1:p.Gly271Ala
|
|
ENST00000276110.6:n.1405G>C
|
|
|
ENST00000374188.7:c.42-295G>C
|
ENSP00000363303.3:n.42-295G>C
|
|
ENST00000374202.6:c.812G>C
|
ENSP00000363318.2:p.Gly271Ala
|
|
ENST00000456850.6:c.242G>C
|
ENSP00000388967.2:p.Gly81Ala
|
|
ENST00000482750.5:c.171-295G>C
|
|
|
ENST00000512747.3:n.739G>C
|
|
|
NM_000206.2:c.812G>C , LRG_150t1:c.812G>C
|
NP_000197.1:p.Gly271Ala
|
|
NM_000206.3:c.812G>C
MANE Select
|
NP_000197.1:p.Gly271Ala
|
|