ENST00000376215.10:c.668G>T
MANE Select
|
ENSP00000365388.5:p.Gly223Val
|
|
ENST00000376215.9:c.668G>T
|
ENSP00000365388.5:p.Gly223Val
|
|
ENST00000473224.1:n.502G>T
|
|
|
ENST00000491711.5:c.76G>T
|
|
|
NM_014317.3:c.668G>T
|
NP_055132.2:p.Gly223Val
|
|
XM_005252439.2:c.158G>T
|
XP_005252496.1:p.Gly53Val
|
|
XM_011519437.1:c.299G>T
|
XP_011517739.1:p.Gly100Val
|
|
XR_428636.2:n.956G>T
|
|
|
XR_930486.1:n.956G>T
|
|
|
NM_001321978.1:c.668G>T
|
NP_001308907.1:p.Gly223Val
|
|
NM_001321979.1:c.158G>T
|
NP_001308908.1:p.Gly53Val
|
|
NM_014317.4:c.668G>T
|
NP_055132.2:p.Gly223Val
|
|
XM_011519437.3:c.299G>T
|
XP_011517739.1:p.Gly100Val
|
|
XM_017016011.2:c.347G>T
|
XP_016871500.1:p.Gly116Val
|
|
XM_024447922.1:c.668G>T
|
XP_024303690.1:p.Gly223Val
|
|
XM_024447923.1:c.158G>T
|
XP_024303691.1:p.Gly53Val
|
|
XR_428636.4:n.956G>T
|
|
|
NM_014317.5:c.668G>T
MANE Select
|
NP_055132.2:p.Gly223Val
|
|
NM_001321978.2:c.668G>T
|
NP_001308907.1:p.Gly223Val
|
|
NM_001321979.2:c.158G>T
|
NP_001308908.1:p.Gly53Val
|
|