ENST00000220420.10:c.747C>G
MANE Select
|
ENSP00000220420.5:p.Gly249=
|
|
ENST00000635871.1:n.216C>G
|
|
|
ENST00000220420.9:c.747C>G
|
ENSP00000220420.5:p.Gly249=
|
|
ENST00000349114.8:c.501C>G
|
ENSP00000220419.8:p.Gly167=
|
|
ENST00000610827.4:c.744C>G
|
ENSP00000479732.1:p.Gly248=
|
|
ENST00000611276.4:c.498C>G
|
ENSP00000482542.1:p.Gly166=
|
|
ENST00000622115.1:c.750C>G
|
ENSP00000479638.1:p.Gly250=
|
|
NM_004245.3:c.501C>G
|
NP_004236.1:p.Gly167=
|
|
NM_201631.3:c.747C>G
|
NP_963925.2:p.Gly249=
|
|
XM_011522229.1:c.747C>G
|
XP_011520531.1:p.Gly249=
|
|
XR_931948.1:n.921C>G
|
|
|
NM_004245.4:c.501C>G
|
NP_004236.1:p.Gly167=
|
|
NM_201631.4:c.747C>G
MANE Select
|
NP_963925.2:p.Gly249=
|
|