ENST00000402696.9:c.801T>A
MANE Select
|
ENSP00000385834.3:p.Ser267=
|
|
ENST00000402696.7:c.801T>A
|
ENSP00000385834.3:p.Ser267=
|
|
ENST00000485977.1:c.166T>A
|
ENSP00000418716.1:p.Ser56Thr
|
|
NM_001063.3:c.801T>A
|
NP_001054.1:p.Ser267=
|
|
XM_011513100.1:c.801T>A
|
XP_011511402.1:p.Ser267=
|
|
NM_001354703.1:c.669T>A
|
NP_001341632.1:p.Ser223=
|
|
NM_001354704.1:c.420T>A
|
NP_001341633.1:p.Ser140=
|
|
NM_001063.4:c.801T>A
MANE Select
|
NP_001054.2:p.Ser267=
|
|
NM_001354703.2:c.669T>A
|
NP_001341632.2:p.Ser223=
|
|
NM_001354704.2:c.420T>A
|
NP_001341633.2:p.Ser140=
|
|