ENST00000645828.1:n.2794C>A
|
|
|
ENST00000651671.1:c.4987C>A
MANE Select
|
ENSP00000498587.1:p.Arg1663=
|
|
ENST00000679595.1:c.4987C>A
|
ENSP00000506241.1:p.Arg1663=
|
|
ENST00000680133.1:c.4873C>A
|
ENSP00000505319.1:p.Arg1625=
|
|
ENST00000680218.1:c.4867C>A
|
ENSP00000505339.1:p.Arg1623=
|
|
ENST00000680668.1:c.4873C>A
|
ENSP00000506336.1:p.Arg1625=
|
|
ENST00000680778.1:c.2584C>A
|
ENSP00000506033.1:p.Arg862=
|
|
ENST00000680924.1:c.*2387C>A
|
ENSP00000506031.1:n.*2387C>A
|
|
ENST00000681135.1:c.*2596C>A
|
ENSP00000506636.1:n.*2596C>A
|
|
ENST00000681298.1:n.1800C>A
|
|
|
ENST00000681454.1:c.*4223C>A
|
ENSP00000505763.1:n.*4223C>A
|
|
ENST00000277541.6:c.4987C>A
|
ENSP00000277541.6:p.Arg1663=
|
|
ENST00000494783.1:n.142C>A
|
|
|
NM_017617.3:c.4987C>A
|
NP_060087.3:p.Arg1663=
|
|
XM_011518717.1:c.4288C>A
|
XP_011517019.1:p.Arg1430=
|
|
NM_017617.5:c.4987C>A
MANE Select
|
NP_060087.3:p.Arg1663=
|
|
XM_011518717.2:c.4264C>A
|
XP_011517019.2:p.Arg1422=
|
|