ENST00000682568.1:n.1817T>G
|
|
|
ENST00000682617.1:c.1877T>G
|
ENSP00000507912.1:p.Leu626Arg
|
|
ENST00000682826.1:c.*1053T>G
|
ENSP00000507274.1:n.*1053T>G
|
|
ENST00000682909.1:n.3779T>G
|
|
|
ENST00000683277.1:n.3384T>G
|
|
|
ENST00000683407.1:n.1747T>G
|
|
|
ENST00000683962.1:c.*1433T>G
|
ENSP00000506854.1:n.*1433T>G
|
|
ENST00000311895.8:c.1739T>G
MANE Select
|
ENSP00000310520.7:p.Leu580Arg
|
|
ENST00000311895.7:c.1739T>G
|
ENSP00000310520.7:p.Leu580Arg
|
|
ENST00000389138.7:n.1016T>G
|
|
|
NM_005236.2:c.1739T>G , LRG_463t1:c.1739T>G
|
NP_005227.1:p.Leu580Arg
|
|
XM_011522424.1:c.1877T>G
|
XP_011520726.1:p.Leu626Arg
|
|
XM_011522425.1:c.1196T>G
|
XP_011520727.1:p.Leu399Arg
|
|
XM_011522426.1:c.950T>G
|
XP_011520728.1:p.Leu317Arg
|
|
XM_011522427.1:c.389T>G
|
XP_011520729.1:p.Leu130Arg
|
|
XR_932805.1:n.1898T>G
|
|
|
XM_011522424.3:c.1877T>G
|
XP_011520726.1:p.Leu626Arg
|
|
XM_017023043.2:c.950T>G
|
XP_016878532.1:p.Leu317Arg
|
|
NM_005236.3:c.1739T>G
MANE Select
|
NP_005227.1:p.Leu580Arg
|
|