ENST00000682568.1:n.1743T>C
|
|
|
ENST00000682617.1:c.1803T>C
|
ENSP00000507912.1:p.His601=
|
|
ENST00000682826.1:c.*979T>C
|
ENSP00000507274.1:n.*979T>C
|
|
ENST00000682909.1:n.3705T>C
|
|
|
ENST00000683277.1:n.3310T>C
|
|
|
ENST00000683407.1:n.1673T>C
|
|
|
ENST00000683962.1:c.*1359T>C
|
ENSP00000506854.1:n.*1359T>C
|
|
ENST00000311895.8:c.1665T>C
MANE Select
|
ENSP00000310520.7:p.His555=
|
|
ENST00000311895.7:c.1665T>C
|
ENSP00000310520.7:p.His555=
|
|
ENST00000389138.7:n.942T>C
|
|
|
NM_005236.2:c.1665T>C , LRG_463t1:c.1665T>C
|
NP_005227.1:p.His555=
|
|
XM_011522424.1:c.1803T>C
|
XP_011520726.1:p.His601=
|
|
XM_011522425.1:c.1122T>C
|
XP_011520727.1:p.His374=
|
|
XM_011522426.1:c.876T>C
|
XP_011520728.1:p.His292=
|
|
XM_011522427.1:c.315T>C
|
XP_011520729.1:p.His105=
|
|
XR_932805.1:n.1824T>C
|
|
|
XM_011522424.3:c.1803T>C
|
XP_011520726.1:p.His601=
|
|
XM_017023043.2:c.876T>C
|
XP_016878532.1:p.His292=
|
|
NM_005236.3:c.1665T>C
MANE Select
|
NP_005227.1:p.His555=
|
|