ENST00000402696.9:c.851A>T
MANE Select
|
ENSP00000385834.3:p.Glu284Val
|
|
ENST00000402696.7:c.851A>T
|
ENSP00000385834.3:p.Glu284Val
|
|
ENST00000485977.1:c.216A>T
|
ENSP00000418716.1:p.Gly72=
|
|
NM_001063.3:c.851A>T
|
NP_001054.1:p.Glu284Val
|
|
XM_011513100.1:c.851A>T
|
XP_011511402.1:p.Glu284Val
|
|
NM_001354703.1:c.719A>T
|
NP_001341632.1:p.Glu240Val
|
|
NM_001354704.1:c.470A>T
|
NP_001341633.1:p.Glu157Val
|
|
NM_001063.4:c.851A>T
MANE Select
|
NP_001054.2:p.Glu284Val
|
|
NM_001354703.2:c.719A>T
|
NP_001341632.2:p.Glu240Val
|
|
NM_001354704.2:c.470A>T
|
NP_001341633.2:p.Glu157Val
|
|