ENST00000697044.1:n.662A>G
|
|
|
ENST00000697098.1:n.392A>G
|
|
|
ENST00000697099.1:n.257A>G
|
|
|
ENST00000648670.1:c.439A>G
|
ENSP00000497173.1:p.Ser147Gly
|
|
ENST00000649202.1:n.286A>G
|
|
|
ENST00000649217.2:c.649A>G
MANE Select
|
ENSP00000497997.1:p.Arg217Gly
|
|
ENST00000650045.1:c.649A>G
|
ENSP00000497036.1:p.Arg217Gly
|
|
ENST00000345724.7:c.649A>G
|
ENSP00000304161.3:p.Arg217Gly
|
|
ENST00000348428.7:c.649A>G
|
ENSP00000319279.4:p.Arg217Gly
|
|
NM_006785.3:c.649A>G
|
NP_006776.1:p.Arg217Gly
|
|
NM_173844.2:c.649A>G
|
NP_776216.1:p.Arg217Gly
|
|
XM_011525794.1:c.649A>G
|
XP_011524096.1:p.Arg217Gly
|
|
XR_935190.1:n.873A>G
|
|
|
XR_935538.1:n.78-3324T>C
|
|
|
NM_006785.4:c.649A>G
MANE Select
|
NP_006776.1:p.Arg217Gly
|
|
XR_001753134.1:n.873A>G
|
|
|
XR_001753135.1:n.873A>G
|
|
|
XR_001753136.1:n.873A>G
|
|
|
NM_173844.3:c.649A>G
|
NP_776216.1:p.Arg217Gly
|
|