ENST00000684169.1:c.192A>T
|
ENSP00000506849.1:p.Gly64=
|
|
ENST00000392386.8:c.192A>T
MANE Select
|
ENSP00000376188.2:p.Gly64=
|
|
ENST00000392386.7:c.192A>T
|
ENSP00000376188.2:p.Gly64=
|
|
ENST00000593286.1:n.444A>T
|
|
|
NM_004750.4:c.192A>T
|
NP_004741.1:p.Gly64=
|
|
XM_011528422.1:c.126A>T
|
XP_011526724.1:p.Gly42=
|
|
XM_011528423.1:c.192A>T
|
XP_011526725.1:p.Gly64=
|
|
XM_011528424.1:c.126A>T
|
XP_011526726.1:p.Gly42=
|
|
XM_011528422.2:c.126A>T
|
XP_011526724.1:p.Gly42=
|
|
XM_011528423.2:c.192A>T
|
XP_011526725.1:p.Gly64=
|
|
XM_011528424.3:c.126A>T
|
XP_011526726.1:p.Gly42=
|
|
NM_004750.5:c.192A>T
MANE Select
|
NP_004741.1:p.Gly64=
|
|