ENST00000402696.9:c.827G>T
MANE Select
|
ENSP00000385834.3:p.Gly276Val
|
|
ENST00000402696.7:c.827G>T
|
ENSP00000385834.3:p.Gly276Val
|
|
ENST00000485977.1:c.192G>T
|
ENSP00000418716.1:p.Gly64=
|
|
NM_001063.3:c.827G>T
|
NP_001054.1:p.Gly276Val
|
|
XM_011513100.1:c.827G>T
|
XP_011511402.1:p.Gly276Val
|
|
NM_001354703.1:c.695G>T
|
NP_001341632.1:p.Gly232Val
|
|
NM_001354704.1:c.446G>T
|
NP_001341633.1:p.Gly149Val
|
|
NM_001063.4:c.827G>T
MANE Select
|
NP_001054.2:p.Gly276Val
|
|
NM_001354703.2:c.695G>T
|
NP_001341632.2:p.Gly232Val
|
|
NM_001354704.2:c.446G>T
|
NP_001341633.2:p.Gly149Val
|
|