ENST00000703212.1:n.583T=
|
|
|
ENST00000703213.1:c.168T=
|
ENSP00000515239.1:p.Gly56=
|
|
ENST00000636456.1:c.-96-589T=
|
ENSP00000490379.1:n.-96-589T=
|
|
ENST00000637181.2:c.168T=
MANE Select
|
ENSP00000490618.1:p.Gly56=
|
|
ENST00000367456.5:c.168T=
|
ENSP00000356426.1:p.Gly56=
|
|
ENST00000470466.5:c.168T=
|
ENSP00000432709.1:p.Gly56=
|
|
ENST00000538427.5:c.168T=
|
ENSP00000445752.1:p.Gly56=
|
|
ENST00000606202.1:c.-55T=
|
ENSP00000476139.1:n.-55T=
|
|
NM_001292034.2:c.168T=
|
NP_001278963.1:p.Gly56=
|
|
NM_001292035.2:c.72T=
|
NP_001278964.1:p.Gly24=
|
|
NM_015093.5:c.168T=
|
NP_055908.1:p.Gly56=
|
|
XM_006715403.2:c.168T=
|
XP_006715466.1:p.Gly56=
|
|
XM_011535633.1:c.168T=
|
XP_011533935.1:p.Gly56=
|
|
XM_011535634.1:c.168T=
|
XP_011533936.1:p.Gly56=
|
|
XM_011535633.2:c.168T=
|
XP_011533935.1:p.Gly56=
|
|
XM_017010591.1:c.168T=
|
XP_016866080.1:p.Gly56=
|
|
XM_017010592.2:c.168T=
|
XP_016866081.1:p.Gly56=
|
|
NM_001292034.3:c.168T=
MANE Select
|
NP_001278963.1:p.Gly56=
|
|
NM_001292035.3:c.72T=
|
NP_001278964.1:p.Gly24=
|
|
NM_001369506.1:c.168T=
|
NP_001356435.1:p.Gly56=
|
|
NM_015093.6:c.168T=
|
NP_055908.1:p.Gly56=
|
|