ENST00000249806.11:c.593C>G
MANE Select
|
ENSP00000249806.5:p.Thr198Ser
|
|
ENST00000562767.2:c.84-12081C>G
|
ENSP00000456336.1:n.84-12081C>G
|
|
ENST00000563917.2:n.435C>G
|
|
|
ENST00000565471.6:c.134C>G
|
ENSP00000457384.1:p.Thr45Ser
|
|
ENST00000635747.1:c.*496C>G
|
ENSP00000490627.1:n.*496C>G
|
|
ENST00000636212.1:c.*263C>G
|
ENSP00000489851.1:n.*263C>G
|
|
ENST00000636314.1:c.289C>G
|
ENSP00000490295.1:p.Leu97Val
|
|
ENST00000636674.1:n.1695C>G
|
|
|
ENST00000636964.1:n.2121C>G
|
|
|
ENST00000637054.1:c.198+8827C>G
|
ENSP00000490807.1:n.198+8827C>G
|
|
ENST00000637223.1:c.*307C>G
|
ENSP00000490010.1:n.*307C>G
|
|
ENST00000637329.1:c.562C>G
|
|
|
ENST00000637450.1:c.*247C>G
|
ENSP00000490204.1:n.*247C>G
|
|
ENST00000637494.1:c.305C>G
|
ENSP00000490057.1:p.Thr102Ser
|
|
ENST00000637667.1:c.494C>G
|
ENSP00000489843.1:p.Thr165Ser
|
|
ENST00000637823.1:c.418C>G
|
|
|
ENST00000637888.1:c.198+8827C>G
|
ENSP00000490546.1:n.198+8827C>G
|
|
ENST00000638076.1:c.*196C>G
|
ENSP00000490373.1:n.*196C>G
|
|
ENST00000638144.1:n.236C>G
|
|
|
ENST00000646164.1:c.38+8827C>G
|
|
|
ENST00000249806.9:c.593C>G
|
ENSP00000249806.5:p.Thr198Ser
|
|
ENST00000538696.5:c.689C>G
|
ENSP00000445770.1:p.Thr230Ser
|
|
ENST00000562767.1:c.84-12081C>G
|
ENSP00000456336.1:n.84-12081C>G
|
|
ENST00000563917.1:n.493C>G
|
|
|
ENST00000564752.1:c.619C>G
|
ENSP00000457822.1:p.Leu207Val
|
|
ENST00000565471.5:c.134C>G
|
ENSP00000457384.1:p.Thr45Ser
|
|
ENST00000566347.5:c.404C>G
|
ENSP00000457783.1:p.Thr135Ser
|
|
ENST00000567060.5:c.309C>G
|
ENSP00000454818.1:p.Tyr103Ter
|
|
NM_017882.2:c.593C>G
|
NP_060352.1:p.Thr198Ser
|
|
XR_931861.1:n.815C>G
|
|
|
NM_017882.3:c.593C>G
MANE Select
|
NP_060352.1:p.Thr198Ser
|
|