ENST00000650793.2:n.207A>G
|
|
|
ENST00000697612.1:n.885A>G
|
|
|
ENST00000374881.3:c.174A>G
|
ENSP00000364015.2:p.Glu58=
|
|
ENST00000374882.8:c.186A>G
MANE Select
|
ENSP00000364016.4:p.Glu62=
|
|
ENST00000650411.1:n.1507A>G
|
|
|
ENST00000650793.1:n.207A>G
|
|
|
ENST00000374881.2:c.174A>G
|
ENSP00000364015.2:p.Glu58=
|
|
ENST00000374882.7:c.186A>G
|
ENSP00000364016.3:p.Glu62=
|
|
ENST00000395339.7:c.186A>G
|
ENSP00000378748.3:p.Glu62=
|
|
ENST00000484003.1:n.412A>G
|
|
|
NM_004159.4:c.174A>G
|
NP_004150.1:p.Glu58=
|
|
NM_148919.3:c.186A>G
|
NP_683720.2:p.Glu62=
|
|
NM_148919.4:c.186A>G
MANE Select
|
NP_683720.2:p.Glu62=
|
|
NM_004159.5:c.174A>G
|
NP_004150.1:p.Glu58=
|
|