ENST00000682568.1:n.1806A>C
|
|
|
ENST00000682617.1:c.1866A>C
|
ENSP00000507912.1:p.Arg622Ser
|
|
ENST00000682826.1:c.*1042A>C
|
ENSP00000507274.1:n.*1042A>C
|
|
ENST00000682909.1:n.3768A>C
|
|
|
ENST00000683277.1:n.3373A>C
|
|
|
ENST00000683407.1:n.1736A>C
|
|
|
ENST00000683962.1:c.*1422A>C
|
ENSP00000506854.1:n.*1422A>C
|
|
ENST00000311895.8:c.1728A>C
MANE Select
|
ENSP00000310520.7:p.Arg576Ser
|
|
ENST00000311895.7:c.1728A>C
|
ENSP00000310520.7:p.Arg576Ser
|
|
ENST00000389138.7:n.1005A>C
|
|
|
NM_005236.2:c.1728A>C , LRG_463t1:c.1728A>C
|
NP_005227.1:p.Arg576Ser
|
|
XM_011522424.1:c.1866A>C
|
XP_011520726.1:p.Arg622Ser
|
|
XM_011522425.1:c.1185A>C
|
XP_011520727.1:p.Arg395Ser
|
|
XM_011522426.1:c.939A>C
|
XP_011520728.1:p.Arg313Ser
|
|
XM_011522427.1:c.378A>C
|
XP_011520729.1:p.Arg126Ser
|
|
XR_932805.1:n.1887A>C
|
|
|
XM_011522424.3:c.1866A>C
|
XP_011520726.1:p.Arg622Ser
|
|
XM_017023043.2:c.939A>C
|
XP_016878532.1:p.Arg313Ser
|
|
NM_005236.3:c.1728A>C
MANE Select
|
NP_005227.1:p.Arg576Ser
|
|