ENST00000682568.1:n.1831C>G
|
|
|
ENST00000682617.1:c.1891C>G
|
ENSP00000507912.1:p.Leu631Val
|
|
ENST00000682826.1:c.*1067C>G
|
ENSP00000507274.1:n.*1067C>G
|
|
ENST00000682909.1:n.3793C>G
|
|
|
ENST00000683277.1:n.3398C>G
|
|
|
ENST00000683407.1:n.1761C>G
|
|
|
ENST00000683962.1:c.*1447C>G
|
ENSP00000506854.1:n.*1447C>G
|
|
ENST00000311895.8:c.1753C>G
MANE Select
|
ENSP00000310520.7:p.Leu585Val
|
|
ENST00000311895.7:c.1753C>G
|
ENSP00000310520.7:p.Leu585Val
|
|
ENST00000389138.7:n.1030C>G
|
|
|
NM_005236.2:c.1753C>G , LRG_463t1:c.1753C>G
|
NP_005227.1:p.Leu585Val
|
|
XM_011522424.1:c.1891C>G
|
XP_011520726.1:p.Leu631Val
|
|
XM_011522425.1:c.1210C>G
|
XP_011520727.1:p.Leu404Val
|
|
XM_011522426.1:c.964C>G
|
XP_011520728.1:p.Leu322Val
|
|
XM_011522427.1:c.403C>G
|
XP_011520729.1:p.Leu135Val
|
|
XR_932805.1:n.1912C>G
|
|
|
XM_011522424.3:c.1891C>G
|
XP_011520726.1:p.Leu631Val
|
|
XM_017023043.2:c.964C>G
|
XP_016878532.1:p.Leu322Val
|
|
NM_005236.3:c.1753C>G
MANE Select
|
NP_005227.1:p.Leu585Val
|
|