ENST00000402696.9:c.837G>T
MANE Select
|
ENSP00000385834.3:p.Glu279Asp
|
|
ENST00000402696.7:c.837G>T
|
ENSP00000385834.3:p.Glu279Asp
|
|
ENST00000485977.1:c.202G>T
|
ENSP00000418716.1:p.Gly68Ter
|
|
NM_001063.3:c.837G>T
|
NP_001054.1:p.Glu279Asp
|
|
XM_011513100.1:c.837G>T
|
XP_011511402.1:p.Glu279Asp
|
|
NM_001354703.1:c.705G>T
|
NP_001341632.1:p.Glu235Asp
|
|
NM_001354704.1:c.456G>T
|
NP_001341633.1:p.Glu152Asp
|
|
NM_001063.4:c.837G>T
MANE Select
|
NP_001054.2:p.Glu279Asp
|
|
NM_001354703.2:c.705G>T
|
NP_001341632.2:p.Glu235Asp
|
|
NM_001354704.2:c.456G>T
|
NP_001341633.2:p.Glu152Asp
|
|