ENST00000257904.11:c.630A>G
MANE Select
|
ENSP00000257904.5:p.Arg210=
|
|
ENST00000257904.10:c.630A>G
|
ENSP00000257904.5:p.Arg210=
|
|
ENST00000312990.10:c.278A>G
|
ENSP00000316889.6:p.Glu93Gly
|
|
ENST00000546489.5:c.408A>G
|
ENSP00000447779.1:p.Arg136=
|
|
ENST00000547281.5:c.408A>G
|
ENSP00000447274.1:p.Arg136=
|
|
ENST00000549606.5:c.-157-1154A>G
|
ENSP00000447005.1:n.-157-1154A>G
|
|
ENST00000550419.5:c.523-95A>G
|
ENSP00000448098.1:n.523-95A>G
|
|
ENST00000551888.5:n.456A>G
|
|
|
ENST00000553237.5:c.*269A>G
|
ENSP00000448885.1:n.*269A>G
|
|
NM_000075.3:c.630A>G
|
NP_000066.1:p.Arg210=
|
|
NM_000075.4:c.630A>G
MANE Select
|
NP_000066.1:p.Arg210=
|
|