ENST00000402696.9:c.812T>G
MANE Select
|
ENSP00000385834.3:p.Val271Gly
|
|
ENST00000402696.7:c.812T>G
|
ENSP00000385834.3:p.Val271Gly
|
|
ENST00000485977.1:c.177T>G
|
ENSP00000418716.1:p.Arg59=
|
|
NM_001063.3:c.812T>G
|
NP_001054.1:p.Val271Gly
|
|
XM_011513100.1:c.812T>G
|
XP_011511402.1:p.Val271Gly
|
|
NM_001354703.1:c.680T>G
|
NP_001341632.1:p.Val227Gly
|
|
NM_001354704.1:c.431T>G
|
NP_001341633.1:p.Val144Gly
|
|
NM_001063.4:c.812T>G
MANE Select
|
NP_001054.2:p.Val271Gly
|
|
NM_001354703.2:c.680T>G
|
NP_001341632.2:p.Val227Gly
|
|
NM_001354704.2:c.431T>G
|
NP_001341633.2:p.Val144Gly
|
|