ENST00000650793.2:n.195T>G
|
|
|
ENST00000697612.1:n.873T>G
|
|
|
ENST00000374881.3:c.162T>G
|
ENSP00000364015.2:p.Gly54=
|
|
ENST00000374882.8:c.174T>G
MANE Select
|
ENSP00000364016.4:p.Gly58=
|
|
ENST00000650411.1:n.1495T>G
|
|
|
ENST00000650793.1:n.195T>G
|
|
|
ENST00000374881.2:c.162T>G
|
ENSP00000364015.2:p.Gly54=
|
|
ENST00000374882.7:c.174T>G
|
ENSP00000364016.3:p.Gly58=
|
|
ENST00000395339.7:c.174T>G
|
ENSP00000378748.3:p.Gly58=
|
|
ENST00000484003.1:n.400T>G
|
|
|
NM_004159.4:c.162T>G
|
NP_004150.1:p.Gly54=
|
|
NM_148919.3:c.174T>G
|
NP_683720.2:p.Gly58=
|
|
NM_148919.4:c.174T>G
MANE Select
|
NP_683720.2:p.Gly58=
|
|
NM_004159.5:c.162T>G
|
NP_004150.1:p.Gly54=
|
|