ENST00000682568.1:n.1733C>G
|
|
|
ENST00000682617.1:c.1793C>G
|
ENSP00000507912.1:p.Thr598Ser
|
|
ENST00000682826.1:c.*969C>G
|
ENSP00000507274.1:n.*969C>G
|
|
ENST00000682909.1:n.3695C>G
|
|
|
ENST00000683277.1:n.3300C>G
|
|
|
ENST00000683407.1:n.1663C>G
|
|
|
ENST00000683962.1:c.*1349C>G
|
ENSP00000506854.1:n.*1349C>G
|
|
ENST00000311895.8:c.1655C>G
MANE Select
|
ENSP00000310520.7:p.Thr552Ser
|
|
ENST00000311895.7:c.1655C>G
|
ENSP00000310520.7:p.Thr552Ser
|
|
ENST00000389138.7:n.932C>G
|
|
|
NM_005236.2:c.1655C>G , LRG_463t1:c.1655C>G
|
NP_005227.1:p.Thr552Ser
|
|
XM_011522424.1:c.1793C>G
|
XP_011520726.1:p.Thr598Ser
|
|
XM_011522425.1:c.1112C>G
|
XP_011520727.1:p.Thr371Ser
|
|
XM_011522426.1:c.866C>G
|
XP_011520728.1:p.Thr289Ser
|
|
XM_011522427.1:c.305C>G
|
XP_011520729.1:p.Thr102Ser
|
|
XR_932805.1:n.1814C>G
|
|
|
XM_011522424.3:c.1793C>G
|
XP_011520726.1:p.Thr598Ser
|
|
XM_017023043.2:c.866C>G
|
XP_016878532.1:p.Thr289Ser
|
|
NM_005236.3:c.1655C>G
MANE Select
|
NP_005227.1:p.Thr552Ser
|
|