ENST00000257904.11:c.617A>G
MANE Select
|
ENSP00000257904.5:p.Glu206Gly
|
|
ENST00000257904.10:c.617A>G
|
ENSP00000257904.5:p.Glu206Gly
|
|
ENST00000312990.10:c.265A>G
|
ENSP00000316889.6:p.Arg89Gly
|
|
ENST00000546489.5:c.395A>G
|
ENSP00000447779.1:p.Glu132Gly
|
|
ENST00000547281.5:c.395A>G
|
ENSP00000447274.1:p.Glu132Gly
|
|
ENST00000549606.5:c.-157-1167A>G
|
ENSP00000447005.1:n.-157-1167A>G
|
|
ENST00000550419.5:c.523-108A>G
|
ENSP00000448098.1:n.523-108A>G
|
|
ENST00000551800.5:c.395A>G
|
ENSP00000449391.1:p.Glu132Gly
|
|
ENST00000551888.5:n.443A>G
|
|
|
ENST00000553237.5:c.*256A>G
|
ENSP00000448885.1:n.*256A>G
|
|
NM_000075.3:c.617A>G
|
NP_000066.1:p.Glu206Gly
|
|
NM_000075.4:c.617A>G
MANE Select
|
NP_000066.1:p.Glu206Gly
|
|