ENST00000645828.1:n.2632G>A
|
|
|
ENST00000651671.1:c.4825G>A
MANE Select
|
ENSP00000498587.1:p.Asp1609Asn
|
|
ENST00000679595.1:c.4825G>A
|
ENSP00000506241.1:p.Asp1609Asn
|
|
ENST00000680133.1:c.4711G>A
|
ENSP00000505319.1:p.Asp1571Asn
|
|
ENST00000680218.1:c.4705G>A
|
ENSP00000505339.1:p.Asp1569Asn
|
|
ENST00000680668.1:c.4711G>A
|
ENSP00000506336.1:p.Asp1571Asn
|
|
ENST00000680778.1:c.2422G>A
|
ENSP00000506033.1:p.Asp808Asn
|
|
ENST00000680924.1:c.*2225G>A
|
ENSP00000506031.1:n.*2225G>A
|
|
ENST00000681135.1:c.*2434G>A
|
ENSP00000506636.1:n.*2434G>A
|
|
ENST00000681298.1:n.1638G>A
|
|
|
ENST00000681454.1:c.*4061G>A
|
ENSP00000505763.1:n.*4061G>A
|
|
ENST00000277541.6:c.4825G>A
|
ENSP00000277541.6:p.Asp1609Asn
|
|
NM_017617.3:c.4825G>A
|
NP_060087.3:p.Asp1609Asn
|
|
XM_011518717.1:c.4126G>A
|
XP_011517019.1:p.Asp1376Asn
|
|
NM_017617.5:c.4825G>A
MANE Select
|
NP_060087.3:p.Asp1609Asn
|
|
XM_011518717.2:c.4102G>A
|
XP_011517019.2:p.Asp1368Asn
|
|