ENST00000645828.1:n.2419G>A
|
|
|
ENST00000651671.1:c.4612G>A
MANE Select
|
ENSP00000498587.1:p.Asp1538Asn
|
|
ENST00000679595.1:c.4612G>A
|
ENSP00000506241.1:p.Asp1538Asn
|
|
ENST00000680133.1:c.4498G>A
|
ENSP00000505319.1:p.Asp1500Asn
|
|
ENST00000680218.1:c.4492G>A
|
ENSP00000505339.1:p.Asp1498Asn
|
|
ENST00000680668.1:c.4498G>A
|
ENSP00000506336.1:p.Asp1500Asn
|
|
ENST00000680778.1:c.2209G>A
|
ENSP00000506033.1:p.Asp737Asn
|
|
ENST00000680924.1:c.*2012G>A
|
ENSP00000506031.1:n.*2012G>A
|
|
ENST00000681135.1:c.*2221G>A
|
ENSP00000506636.1:n.*2221G>A
|
|
ENST00000681298.1:n.1425G>A
|
|
|
ENST00000681454.1:c.*3848G>A
|
ENSP00000505763.1:n.*3848G>A
|
|
ENST00000277541.6:c.4612G>A
|
ENSP00000277541.6:p.Asp1538Asn
|
|
NM_017617.3:c.4612G>A
|
NP_060087.3:p.Asp1538Asn
|
|
XM_011518717.1:c.3913G>A
|
XP_011517019.1:p.Asp1305Asn
|
|
NM_017617.5:c.4612G>A
MANE Select
|
NP_060087.3:p.Asp1538Asn
|
|
XM_011518717.2:c.3889G>A
|
XP_011517019.2:p.Asp1297Asn
|
|