ENST00000651671.1:c.6462G>A
MANE Select
|
ENSP00000498587.1:p.Gln2154=
|
|
ENST00000679595.1:c.*1502G>A
|
ENSP00000506241.1:n.*1502G>A
|
|
ENST00000679969.1:n.3058G>A
|
|
|
ENST00000680003.1:n.2794G>A
|
|
|
ENST00000680133.1:c.6348G>A
|
ENSP00000505319.1:p.Gln2116=
|
|
ENST00000680218.1:c.6342G>A
|
ENSP00000505339.1:p.Gln2114=
|
|
ENST00000680668.1:c.6348G>A
|
ENSP00000506336.1:p.Gln2116=
|
|
ENST00000680778.1:c.4059G>A
|
ENSP00000506033.1:p.Gln1353=
|
|
ENST00000680924.1:c.*3862G>A
|
ENSP00000506031.1:n.*3862G>A
|
|
ENST00000681135.1:c.*4071G>A
|
ENSP00000506636.1:n.*4071G>A
|
|
ENST00000681298.1:n.4567G>A
|
|
|
ENST00000681454.1:c.*5698G>A
|
ENSP00000505763.1:n.*5698G>A
|
|
ENST00000277541.6:c.6462G>A
|
ENSP00000277541.6:p.Gln2154=
|
|
NM_017617.3:c.6462G>A
|
NP_060087.3:p.Gln2154=
|
|
XM_011518717.1:c.5763G>A
|
XP_011517019.1:p.Gln1921=
|
|
NM_017617.5:c.6462G>A
MANE Select
|
NP_060087.3:p.Gln2154=
|
|
XM_011518717.2:c.5739G>A
|
XP_011517019.2:p.Gln1913=
|
|