ENST00000309755.9:c.1490G=
MANE Select
|
ENSP00000312397.4:p.Gly497=
|
|
ENST00000309755.8:c.1490G=
|
ENSP00000312397.4:p.Gly497=
|
|
ENST00000447439.6:n.1546G=
|
|
|
ENST00000504208.5:c.*374G=
|
ENSP00000423585.1:n.*374G=
|
|
ENST00000506491.5:c.1244G=
|
ENSP00000424828.1:p.Gly415=
|
|
ENST00000506873.5:n.1013G=
|
|
|
ENST00000508657.5:c.1394G=
|
ENSP00000422099.1:p.Gly465=
|
|
ENST00000509694.1:n.283G=
|
|
|
NM_001257194.1:c.1394G=
|
NP_001244123.1:p.Gly465=
|
|
NM_001257195.1:c.1244G=
|
NP_001244124.1:p.Gly415=
|
|
NM_017415.2:c.1490G=
|
NP_059111.2:p.Gly497=
|
|
NM_017415.3:c.1490G=
MANE Select
|
NP_059111.2:p.Gly497=
|
|
NM_001257195.2:c.1244G=
|
NP_001244124.1:p.Gly415=
|
|