ENST00000651671.1:c.6076G>A
MANE Select
|
ENSP00000498587.1:p.Asp2026Asn
|
|
ENST00000679595.1:c.*1116G>A
|
ENSP00000506241.1:n.*1116G>A
|
|
ENST00000679969.1:n.2557G>A
|
|
|
ENST00000680003.1:n.2408G>A
|
|
|
ENST00000680133.1:c.5962G>A
|
ENSP00000505319.1:p.Asp1988Asn
|
|
ENST00000680218.1:c.5956G>A
|
ENSP00000505339.1:p.Asp1986Asn
|
|
ENST00000680668.1:c.5962G>A
|
ENSP00000506336.1:p.Asp1988Asn
|
|
ENST00000680778.1:c.3673G>A
|
ENSP00000506033.1:p.Asp1225Asn
|
|
ENST00000680924.1:c.*3476G>A
|
ENSP00000506031.1:n.*3476G>A
|
|
ENST00000681135.1:c.*3685G>A
|
ENSP00000506636.1:n.*3685G>A
|
|
ENST00000681298.1:n.4181G>A
|
|
|
ENST00000681454.1:c.*5312G>A
|
ENSP00000505763.1:n.*5312G>A
|
|
ENST00000277541.6:c.6076G>A
|
ENSP00000277541.6:p.Asp2026Asn
|
|
NM_017617.3:c.6076G>A
|
NP_060087.3:p.Asp2026Asn
|
|
XM_011518717.1:c.5377G>A
|
XP_011517019.1:p.Asp1793Asn
|
|
NM_017617.5:c.6076G>A
MANE Select
|
NP_060087.3:p.Asp2026Asn
|
|
XM_011518717.2:c.5353G>A
|
XP_011517019.2:p.Asp1785Asn
|
|