ENST00000220616.9:c.8181A>C
MANE Select
|
ENSP00000220616.4:p.Thr2727=
|
|
ENST00000220616.8:c.8181A>C
|
ENSP00000220616.4:p.Thr2727=
|
|
ENST00000519178.5:c.3547A>C
|
|
|
ENST00000519543.5:c.2580A>C
|
ENSP00000430430.1:p.Thr860=
|
|
ENST00000521107.1:c.393A>C
|
ENSP00000430161.1:p.Thr131=
|
|
ENST00000522691.1:n.267A>C
|
|
|
ENST00000523756.5:c.4836A>C
|
|
|
NM_003235.4:c.8181A>C
|
NP_003226.4:p.Thr2727=
|
|
XM_005251038.3:c.7989A>C
|
XP_005251095.1:p.Thr2663=
|
|
XM_006716622.2:c.8118A>C
|
XP_006716685.1:p.Thr2706=
|
|
XM_005251038.4:c.7989A>C
|
XP_005251095.1:p.Thr2663=
|
|
XM_006716622.3:c.8118A>C
|
XP_006716685.1:p.Thr2706=
|
|
XM_017013793.1:c.8115A>C
|
XP_016869282.1:p.Thr2705=
|
|
XM_017013794.1:c.8046A>C
|
XP_016869283.1:p.Thr2682=
|
|
XM_017013795.1:c.8010A>C
|
XP_016869284.1:p.Thr2670=
|
|
XM_017013796.1:c.7962A>C
|
XP_016869285.1:p.Thr2654=
|
|
XM_017013797.1:c.7920A>C
|
XP_016869286.1:p.Thr2640=
|
|
NM_003235.5:c.8181A>C
MANE Select
|
NP_003226.4:p.Thr2727=
|
|