ENST00000645828.1:n.2739G>T
|
|
|
ENST00000651671.1:c.4932G>T
MANE Select
|
ENSP00000498587.1:p.Leu1644=
|
|
ENST00000679595.1:c.4932G>T
|
ENSP00000506241.1:p.Leu1644=
|
|
ENST00000680133.1:c.4818G>T
|
ENSP00000505319.1:p.Leu1606=
|
|
ENST00000680218.1:c.4812G>T
|
ENSP00000505339.1:p.Leu1604=
|
|
ENST00000680668.1:c.4818G>T
|
ENSP00000506336.1:p.Leu1606=
|
|
ENST00000680778.1:c.2529G>T
|
ENSP00000506033.1:p.Leu843=
|
|
ENST00000680924.1:c.*2332G>T
|
ENSP00000506031.1:n.*2332G>T
|
|
ENST00000681135.1:c.*2541G>T
|
ENSP00000506636.1:n.*2541G>T
|
|
ENST00000681298.1:n.1745G>T
|
|
|
ENST00000681454.1:c.*4168G>T
|
ENSP00000505763.1:n.*4168G>T
|
|
ENST00000277541.6:c.4932G>T
|
ENSP00000277541.6:p.Leu1644=
|
|
ENST00000494783.1:n.87G>T
|
|
|
NM_017617.3:c.4932G>T
|
NP_060087.3:p.Leu1644=
|
|
XM_011518717.1:c.4233G>T
|
XP_011517019.1:p.Leu1411=
|
|
NM_017617.5:c.4932G>T
MANE Select
|
NP_060087.3:p.Leu1644=
|
|
XM_011518717.2:c.4209G>T
|
XP_011517019.2:p.Leu1403=
|
|