ENST00000682568.1:n.1774C>T
|
|
|
ENST00000682617.1:c.1834C>T
|
ENSP00000507912.1:p.Leu612=
|
|
ENST00000682826.1:c.*1010C>T
|
ENSP00000507274.1:n.*1010C>T
|
|
ENST00000682909.1:n.3736C>T
|
|
|
ENST00000683277.1:n.3341C>T
|
|
|
ENST00000683407.1:n.1704C>T
|
|
|
ENST00000683962.1:c.*1390C>T
|
ENSP00000506854.1:n.*1390C>T
|
|
ENST00000311895.8:c.1696C>T
MANE Select
|
ENSP00000310520.7:p.Leu566=
|
|
ENST00000311895.7:c.1696C>T
|
ENSP00000310520.7:p.Leu566=
|
|
ENST00000389138.7:n.973C>T
|
|
|
NM_005236.2:c.1696C>T , LRG_463t1:c.1696C>T
|
NP_005227.1:p.Leu566=
|
|
XM_011522424.1:c.1834C>T
|
XP_011520726.1:p.Leu612=
|
|
XM_011522425.1:c.1153C>T
|
XP_011520727.1:p.Leu385=
|
|
XM_011522426.1:c.907C>T
|
XP_011520728.1:p.Leu303=
|
|
XM_011522427.1:c.346C>T
|
XP_011520729.1:p.Leu116=
|
|
XR_932805.1:n.1855C>T
|
|
|
XM_011522424.3:c.1834C>T
|
XP_011520726.1:p.Leu612=
|
|
XM_017023043.2:c.907C>T
|
XP_016878532.1:p.Leu303=
|
|
NM_005236.3:c.1696C>T
MANE Select
|
NP_005227.1:p.Leu566=
|
|