ENST00000470094.2:c.*329G>C
|
ENSP00000434898.2:n.*329G>C
|
|
ENST00000528762.2:c.*1173G>C
|
ENSP00000433168.2:n.*1173G>C
|
|
ENST00000530893.7:c.9437G>C
|
ENSP00000499438.2:p.Arg3146Thr
|
|
ENST00000665585.2:c.*1368G>C
|
ENSP00000499570.2:n.*1368G>C
|
|
ENST00000700202.2:c.9755G>C
|
ENSP00000514856.2:p.Arg3252Thr
|
|
ENST00000700202.1:c.2222G>C
|
ENSP00000514856.1:p.Arg741Thr
|
|
ENST00000700203.1:n.1933G>C
|
|
|
ENST00000380152.8:c.9806G>C
MANE Select
|
ENSP00000369497.3:p.Arg3269Thr
|
|
ENST00000544455.6:c.9806G>C
|
ENSP00000439902.1:p.Arg3269Thr
|
|
ENST00000614259.2:c.9814G>C
|
ENSP00000506251.1:n.9814G>C
|
|
ENST00000680887.1:c.9806G>C
|
ENSP00000505508.1:p.Arg3269Thr
|
|
ENST00000380152.7:c.9806G>C
|
ENSP00000369497.3:p.Arg3269Thr
|
|
ENST00000533776.1:n.394G>C
|
|
|
ENST00000544455.5:c.9806G>C
|
ENSP00000439902.1:p.Arg3269Thr
|
|
NM_000059.3:c.9806G>C , LRG_293t1:c.9806G>C
|
NP_000050.2:p.Arg3269Thr
|
|
XM_011535203.1:c.9806G>C
|
XP_011533505.1:p.Arg3269Thr
|
|
XM_011535204.1:c.9710G>C
|
XP_011533506.1:p.Arg3237Thr
|
|
NM_000059.4:c.9806G>C
MANE Select
|
NP_000050.3:p.Arg3269Thr
|
|