ENST00000645828.1:n.2734G>A
|
|
|
ENST00000651671.1:c.4927G>A
MANE Select
|
ENSP00000498587.1:p.Ala1643Thr
|
|
ENST00000679595.1:c.4927G>A
|
ENSP00000506241.1:p.Ala1643Thr
|
|
ENST00000680133.1:c.4813G>A
|
ENSP00000505319.1:p.Ala1605Thr
|
|
ENST00000680218.1:c.4807G>A
|
ENSP00000505339.1:p.Ala1603Thr
|
|
ENST00000680668.1:c.4813G>A
|
ENSP00000506336.1:p.Ala1605Thr
|
|
ENST00000680778.1:c.2524G>A
|
ENSP00000506033.1:p.Ala842Thr
|
|
ENST00000680924.1:c.*2327G>A
|
ENSP00000506031.1:n.*2327G>A
|
|
ENST00000681135.1:c.*2536G>A
|
ENSP00000506636.1:n.*2536G>A
|
|
ENST00000681298.1:n.1740G>A
|
|
|
ENST00000681454.1:c.*4163G>A
|
ENSP00000505763.1:n.*4163G>A
|
|
ENST00000277541.6:c.4927G>A
|
ENSP00000277541.6:p.Ala1643Thr
|
|
ENST00000494783.1:n.82G>A
|
|
|
NM_017617.3:c.4927G>A
|
NP_060087.3:p.Ala1643Thr
|
|
XM_011518717.1:c.4228G>A
|
XP_011517019.1:p.Ala1410Thr
|
|
NM_017617.5:c.4927G>A
MANE Select
|
NP_060087.3:p.Ala1643Thr
|
|
XM_011518717.2:c.4204G>A
|
XP_011517019.2:p.Ala1402Thr
|
|