ENST00000682617.1:c.2140G=
|
ENSP00000507912.1:p.Asp714=
|
|
ENST00000683962.1:c.*1696G=
|
ENSP00000506854.1:n.*1696G=
|
|
ENST00000311895.8:c.2002G=
MANE Select
|
ENSP00000310520.7:p.Asp668=
|
|
ENST00000311895.7:c.2002G=
|
ENSP00000310520.7:p.Asp668=
|
|
ENST00000389138.7:n.1279G=
|
|
|
ENST00000462862.1:c.315G=
|
ENSP00000461322.1:n.315G=
|
|
NM_005236.2:c.2002G= , LRG_463t1:c.2002G=
|
NP_005227.1:p.Asp668=
|
|
XM_011522424.1:c.2140G=
|
XP_011520726.1:p.Asp714=
|
|
XM_011522425.1:c.1459G=
|
XP_011520727.1:p.Asp487=
|
|
XM_011522426.1:c.1213G=
|
XP_011520728.1:p.Asp405=
|
|
XM_011522427.1:c.652G=
|
XP_011520729.1:p.Asp218=
|
|
XR_932805.1:n.2161G=
|
|
|
XM_011522424.3:c.2140G=
|
XP_011520726.1:p.Asp714=
|
|
XM_017023043.2:c.1213G=
|
XP_016878532.1:p.Asp405=
|
|
NM_005236.3:c.2002G=
MANE Select
|
NP_005227.1:p.Asp668=
|
|