ENST00000249806.11:c.530G>T
MANE Select
|
ENSP00000249806.5:p.Gly177Val
|
|
ENST00000562767.2:c.84-13647G>T
|
ENSP00000456336.1:n.84-13647G>T
|
|
ENST00000563917.2:n.372G>T
|
|
|
ENST00000565471.6:c.84-1516G>T
|
ENSP00000457384.1:n.84-1516G>T
|
|
ENST00000635747.1:c.*433G>T
|
ENSP00000490627.1:n.*433G>T
|
|
ENST00000636212.1:c.*200G>T
|
ENSP00000489851.1:n.*200G>T
|
|
ENST00000636314.1:c.226G>T
|
ENSP00000490295.1:p.Val76Phe
|
|
ENST00000636674.1:n.1632G>T
|
|
|
ENST00000636964.1:n.2058G>T
|
|
|
ENST00000637054.1:c.198+7261G>T
|
ENSP00000490807.1:n.198+7261G>T
|
|
ENST00000637223.1:c.*244G>T
|
ENSP00000490010.1:n.*244G>T
|
|
ENST00000637329.1:c.499G>T
|
|
|
ENST00000637450.1:c.*184G>T
|
ENSP00000490204.1:n.*184G>T
|
|
ENST00000637494.1:c.242G>T
|
ENSP00000490057.1:p.Gly81Val
|
|
ENST00000637667.1:c.431G>T
|
ENSP00000489843.1:p.Gly144Val
|
|
ENST00000637823.1:c.355G>T
|
|
|
ENST00000637888.1:c.198+7261G>T
|
ENSP00000490546.1:n.198+7261G>T
|
|
ENST00000638076.1:c.*133G>T
|
ENSP00000490373.1:n.*133G>T
|
|
ENST00000638144.1:n.173G>T
|
|
|
ENST00000646164.1:c.38+7261G>T
|
|
|
ENST00000249806.9:c.530G>T
|
ENSP00000249806.5:p.Gly177Val
|
|
ENST00000538696.5:c.626G>T
|
ENSP00000445770.1:p.Gly209Val
|
|
ENST00000562767.1:c.84-13647G>T
|
ENSP00000456336.1:n.84-13647G>T
|
|
ENST00000563917.1:n.430G>T
|
|
|
ENST00000564752.1:c.556G>T
|
ENSP00000457822.1:p.Val186Phe
|
|
ENST00000565471.5:c.84-1516G>T
|
ENSP00000457384.1:n.84-1516G>T
|
|
ENST00000566347.5:c.341G>T
|
ENSP00000457783.1:p.Gly114Val
|
|
ENST00000567060.5:c.298-1555G>T
|
ENSP00000454818.1:n.298-1555G>T
|
|
NM_017882.2:c.530G>T
|
NP_060352.1:p.Gly177Val
|
|
XR_931861.1:n.752G>T
|
|
|
NM_017882.3:c.530G>T
MANE Select
|
NP_060352.1:p.Gly177Val
|
|