ENST00000682114.1:c.572+94G=
|
ENSP00000507245.1:n.572+94G=
|
|
ENST00000682478.1:n.762+94G=
|
|
|
ENST00000683576.1:n.856G=
|
|
|
ENST00000683627.1:c.666G=
|
ENSP00000507533.1:p.Gln222=
|
|
ENST00000684082.1:c.623G=
|
ENSP00000508266.1:n.623G=
|
|
ENST00000684633.1:n.638G=
|
|
|
ENST00000684678.1:c.568+94G=
|
ENSP00000507059.1:n.568+94G=
|
|
ENST00000369842.9:c.666G=
MANE Select
|
ENSP00000358857.4:p.Gln222=
|
|
ENST00000369835.3:c.561G=
|
ENSP00000358850.3:p.Gln187=
|
|
ENST00000369842.8:c.666G=
|
ENSP00000358857.4:p.Gln222=
|
|
ENST00000428228.5:c.*571G=
|
ENSP00000401081.1:n.*571G=
|
|
ENST00000471965.1:n.455G=
|
|
|
ENST00000486738.5:n.1103G=
|
|
|
ENST00000492448.1:n.649G=
|
|
|
NM_000117.2:c.666G= , LRG_745t1:c.666G=
|
NP_000108.1:p.Gln222=
|
|
XM_024452349.1:c.672G=
|
XP_024308117.1:p.Gln224=
|
|
NM_000117.3:c.666G=
MANE Select
|
NP_000108.1:p.Gln222=
|
|