ENST00000651671.1:c.6574G=
MANE Select
|
ENSP00000498587.1:p.Asp2192=
|
|
ENST00000679595.1:c.*1614G=
|
ENSP00000506241.1:n.*1614G=
|
|
ENST00000679969.1:n.3170G=
|
|
|
ENST00000680003.1:n.2906G=
|
|
|
ENST00000680133.1:c.6460G=
|
ENSP00000505319.1:p.Asp2154=
|
|
ENST00000680218.1:c.6454G=
|
ENSP00000505339.1:p.Asp2152=
|
|
ENST00000680668.1:c.6460G=
|
ENSP00000506336.1:p.Asp2154=
|
|
ENST00000680778.1:c.4171G=
|
ENSP00000506033.1:p.Asp1391=
|
|
ENST00000680924.1:c.*3974G=
|
ENSP00000506031.1:n.*3974G=
|
|
ENST00000681135.1:c.*4183G=
|
ENSP00000506636.1:n.*4183G=
|
|
ENST00000681298.1:n.4679G=
|
|
|
ENST00000681454.1:c.*5810G=
|
ENSP00000505763.1:n.*5810G=
|
|
ENST00000277541.6:c.6574G=
|
ENSP00000277541.6:p.Asp2192=
|
|
NM_017617.3:c.6574G=
|
NP_060087.3:p.Asp2192=
|
|
XM_011518717.1:c.5875G=
|
XP_011517019.1:p.Asp1959=
|
|
NM_017617.5:c.6574G=
MANE Select
|
NP_060087.3:p.Asp2192=
|
|
XM_011518717.2:c.5851G=
|
XP_011517019.2:p.Asp1951=
|
|