ENST00000697124.1:n.1110A>C
|
|
|
ENST00000219596.6:c.1989A>C
MANE Select
|
ENSP00000219596.1:p.Thr663=
|
|
ENST00000219596.5:c.1989A>C
|
ENSP00000219596.1:p.Thr663=
|
|
ENST00000339854.8:c.1449A>C
|
ENSP00000339639.4:p.Thr483=
|
|
ENST00000536379.5:c.1356A>C
|
ENSP00000445079.1:p.Thr452=
|
|
ENST00000536980.5:c.*265A>C
|
ENSP00000444178.1:n.*265A>C
|
|
ENST00000537682.5:c.*265A>C
|
ENSP00000438611.1:n.*265A>C
|
|
ENST00000538326.5:c.*614A>C
|
ENSP00000437486.1:n.*614A>C
|
|
ENST00000539145.5:c.910A>C
|
ENSP00000444471.1:n.910A>C
|
|
ENST00000541159.5:c.1531A>C
|
ENSP00000438711.1:n.1531A>C
|
|
ENST00000542898.5:c.*265A>C
|
ENSP00000444615.1:n.*265A>C
|
|
ENST00000570511.5:c.1394A>C
|
ENSP00000458312.1:n.1394A>C
|
|
ENST00000572244.5:c.679A>C
|
ENSP00000461186.1:n.679A>C
|
|
ENST00000574583.5:c.761A>C
|
ENSP00000460269.1:n.761A>C
|
|
ENST00000576315.5:c.794A>C
|
ENSP00000460551.1:n.794A>C
|
|
ENST00000621655.1:c.1526A>C
|
ENSP00000481436.1:n.1526A>C
|
|
NM_000243.2:c.1989A>C , LRG_190t1:c.1989A>C
|
NP_000234.1:p.Thr663=
|
|
NM_001198536.1:c.*193A>C
|
NP_001185465.1:n.*193A>C
|
|
XM_017023236.2:c.1986A>C
|
XP_016878725.1:p.Thr662=
|
|
NM_000243.3:c.1989A>C
MANE Select
|
NP_000234.1:p.Thr663=
|
|
NM_001198536.2:c.*193A>C
|
NP_001185465.2:n.*193A>C
|
|