ENST00000261208.8:c.755G=
MANE Select
|
ENSP00000261208.3:p.Gly252=
|
|
ENST00000261208.7:c.755G=
|
ENSP00000261208.3:p.Gly252=
|
|
ENST00000538703.5:c.755G=
|
ENSP00000440861.1:p.Gly252=
|
|
ENST00000541929.5:c.131G=
|
ENSP00000446364.1:p.Gly44=
|
|
ENST00000544080.6:c.*184G=
|
ENSP00000439385.2:n.*184G=
|
|
ENST00000546999.5:c.*184G=
|
ENSP00000447675.1:n.*184G=
|
|
ENST00000549376.1:n.148G=
|
|
|
ENST00000551562.1:n.15G=
|
|
|
ENST00000552509.5:c.719G=
|
ENSP00000450372.1:p.Gly240=
|
|
NM_001258333.1:c.131G=
|
NP_001245262.1:p.Gly44=
|
|
NM_001258334.1:c.755G=
|
NP_001245263.1:p.Gly252=
|
|
NM_002108.3:c.755G=
|
NP_002099.1:p.Gly252=
|
|
XM_011538249.1:c.3+2187G=
|
XP_011536551.1:n.3+2187G=
|
|
XM_011538249.2:c.3+2187G=
|
XP_011536551.1:n.3+2187G=
|
|
NM_002108.4:c.755G=
MANE Select
|
NP_002099.1:p.Gly252=
|
|
NM_001258334.2:c.755G=
|
NP_001245263.1:p.Gly252=
|
|
NM_001258333.2:c.131G=
|
NP_001245262.1:p.Gly44=
|
|