ENST00000682114.1:c.445G=
|
ENSP00000507245.1:p.Asp149=
|
|
ENST00000682478.1:n.635G=
|
|
|
ENST00000683576.1:n.635G=
|
|
|
ENST00000683627.1:c.445G=
|
ENSP00000507533.1:p.Asp149=
|
|
ENST00000684082.1:c.402G=
|
ENSP00000508266.1:n.402G=
|
|
ENST00000684633.1:n.417G=
|
|
|
ENST00000684678.1:c.441G=
|
ENSP00000507059.1:n.441G=
|
|
ENST00000369842.9:c.445G=
MANE Select
|
ENSP00000358857.4:p.Asp149=
|
|
ENST00000369835.3:c.340G=
|
ENSP00000358850.3:p.Asp114=
|
|
ENST00000369842.8:c.445G=
|
ENSP00000358857.4:p.Asp149=
|
|
ENST00000428228.5:c.*350G=
|
ENSP00000401081.1:n.*350G=
|
|
ENST00000468294.5:n.405G=
|
|
|
ENST00000471965.1:n.234G=
|
|
|
ENST00000485261.1:n.635G=
|
|
|
ENST00000486738.5:n.803G=
|
|
|
ENST00000492448.1:n.428G=
|
|
|
NM_000117.2:c.445G= , LRG_745t1:c.445G=
|
NP_000108.1:p.Asp149=
|
|
XM_024452349.1:c.451G=
|
XP_024308117.1:p.Asp151=
|
|
NM_000117.3:c.445G=
MANE Select
|
NP_000108.1:p.Asp149=
|
|