ENST00000645828.1:n.2732A>T
|
|
|
ENST00000651671.1:c.4925A>T
MANE Select
|
ENSP00000498587.1:p.Asp1642Val
|
|
ENST00000679595.1:c.4925A>T
|
ENSP00000506241.1:p.Asp1642Val
|
|
ENST00000680133.1:c.4811A>T
|
ENSP00000505319.1:p.Asp1604Val
|
|
ENST00000680218.1:c.4805A>T
|
ENSP00000505339.1:p.Asp1602Val
|
|
ENST00000680668.1:c.4811A>T
|
ENSP00000506336.1:p.Asp1604Val
|
|
ENST00000680778.1:c.2522A>T
|
ENSP00000506033.1:p.Asp841Val
|
|
ENST00000680924.1:c.*2325A>T
|
ENSP00000506031.1:n.*2325A>T
|
|
ENST00000681135.1:c.*2534A>T
|
ENSP00000506636.1:n.*2534A>T
|
|
ENST00000681298.1:n.1738A>T
|
|
|
ENST00000681454.1:c.*4161A>T
|
ENSP00000505763.1:n.*4161A>T
|
|
ENST00000277541.6:c.4925A>T
|
ENSP00000277541.6:p.Asp1642Val
|
|
ENST00000494783.1:n.80A>T
|
|
|
NM_017617.3:c.4925A>T
|
NP_060087.3:p.Asp1642Val
|
|
XM_011518717.1:c.4226A>T
|
XP_011517019.1:p.Asp1409Val
|
|
NM_017617.5:c.4925A>T
MANE Select
|
NP_060087.3:p.Asp1642Val
|
|
XM_011518717.2:c.4202A>T
|
XP_011517019.2:p.Asp1401Val
|
|