ENST00000682568.1:n.1746G>T
|
|
|
ENST00000682617.1:c.1806G>T
|
ENSP00000507912.1:p.Pro602=
|
|
ENST00000682826.1:c.*982G>T
|
ENSP00000507274.1:n.*982G>T
|
|
ENST00000682909.1:n.3708G>T
|
|
|
ENST00000683277.1:n.3313G>T
|
|
|
ENST00000683407.1:n.1676G>T
|
|
|
ENST00000683962.1:c.*1362G>T
|
ENSP00000506854.1:n.*1362G>T
|
|
ENST00000311895.8:c.1668G>T
MANE Select
|
ENSP00000310520.7:p.Pro556=
|
|
ENST00000311895.7:c.1668G>T
|
ENSP00000310520.7:p.Pro556=
|
|
ENST00000389138.7:n.945G>T
|
|
|
NM_005236.2:c.1668G>T , LRG_463t1:c.1668G>T
|
NP_005227.1:p.Pro556=
|
|
XM_011522424.1:c.1806G>T
|
XP_011520726.1:p.Pro602=
|
|
XM_011522425.1:c.1125G>T
|
XP_011520727.1:p.Pro375=
|
|
XM_011522426.1:c.879G>T
|
XP_011520728.1:p.Pro293=
|
|
XM_011522427.1:c.318G>T
|
XP_011520729.1:p.Pro106=
|
|
XR_932805.1:n.1827G>T
|
|
|
XM_011522424.3:c.1806G>T
|
XP_011520726.1:p.Pro602=
|
|
XM_017023043.2:c.879G>T
|
XP_016878532.1:p.Pro293=
|
|
NM_005236.3:c.1668G>T
MANE Select
|
NP_005227.1:p.Pro556=
|
|