ENST00000318227.4:c.770A>C
|
ENSP00000314879.4:p.Lys257Thr
|
|
ENST00000380149.6:c.770A>C
|
ENSP00000369494.2:p.Lys257Thr
|
|
ENST00000448843.7:c.770A>C
MANE Select
|
ENSP00000400581.2:p.Lys257Thr
|
|
ENST00000318227.3:c.1166A>C
|
ENSP00000314879.3:p.Lys389Thr
|
|
ENST00000380149.5:c.1238A>C
|
ENSP00000369494.1:p.Lys413Thr
|
|
ENST00000448843.6:c.770A>C
|
ENSP00000400581.2:p.Lys257Thr
|
|
NM_001165960.1:c.1166A>C
|
NP_001159432.1:p.Lys389Thr
|
|
NM_021628.2:c.770A>C
|
NP_067641.2:p.Lys257Thr
|
|
XM_017024921.2:c.770A>C
|
XP_016880410.1:p.Lys257Thr
|
|
XM_017024922.2:c.770A>C
|
XP_016880411.1:p.Lys257Thr
|
|
XM_017024923.2:c.770A>C
|
XP_016880412.1:p.Lys257Thr
|
|
XM_017024924.2:c.770A>C
|
XP_016880413.1:p.Lys257Thr
|
|
XM_017024925.2:c.770A>C
|
XP_016880414.1:p.Lys257Thr
|
|
XR_001752579.2:n.1043A>C
|
|
|
XR_001752580.2:n.1043A>C
|
|
|
NM_001369446.1:c.767A>C
|
NP_001356375.1:p.Lys256Thr
|
|
NM_021628.3:c.770A>C
MANE Select
|
NP_067641.2:p.Lys257Thr
|
|