ENST00000682568.1:n.1665T>C
|
|
|
ENST00000682617.1:c.1725T>C
|
ENSP00000507912.1:p.Ile575=
|
|
ENST00000682826.1:c.*901T>C
|
ENSP00000507274.1:n.*901T>C
|
|
ENST00000682909.1:n.3627T>C
|
|
|
ENST00000683277.1:n.3232T>C
|
|
|
ENST00000683407.1:n.1595T>C
|
|
|
ENST00000683962.1:c.*1281T>C
|
ENSP00000506854.1:n.*1281T>C
|
|
ENST00000311895.8:c.1587T>C
MANE Select
|
ENSP00000310520.7:p.Ile529=
|
|
ENST00000311895.7:c.1587T>C
|
ENSP00000310520.7:p.Ile529=
|
|
ENST00000389138.7:n.864T>C
|
|
|
NM_005236.2:c.1587T>C , LRG_463t1:c.1587T>C
|
NP_005227.1:p.Ile529=
|
|
XM_011522424.1:c.1725T>C
|
XP_011520726.1:p.Ile575=
|
|
XM_011522425.1:c.1044T>C
|
XP_011520727.1:p.Ile348=
|
|
XM_011522426.1:c.798T>C
|
XP_011520728.1:p.Ile266=
|
|
XM_011522427.1:c.237T>C
|
XP_011520729.1:p.Ile79=
|
|
XR_932805.1:n.1746T>C
|
|
|
XM_011522424.3:c.1725T>C
|
XP_011520726.1:p.Ile575=
|
|
XM_017023043.2:c.798T>C
|
XP_016878532.1:p.Ile266=
|
|
NM_005236.3:c.1587T>C
MANE Select
|
NP_005227.1:p.Ile529=
|
|