ENST00000643759.2:c.7052T>A
MANE Select
|
ENSP00000495214.1:p.Ile2351Asn
|
|
ENST00000368147.8:c.7052T>A
|
ENSP00000357129.4:p.Ile2351Asn
|
|
ENST00000481212.5:n.493T>A
|
|
|
ENST00000498708.1:n.484T>A
|
|
|
ENST00000614909.4:c.7052T>A
|
ENSP00000482595.1:p.Ile2351Asn
|
|
NM_003126.2:c.7052T>A
|
NP_003117.2:p.Ile2351Asn
|
|
XM_011509916.1:c.7052T>A
|
XP_011508218.1:p.Ile2351Asn
|
|
XM_011509917.1:c.7034T>A
|
XP_011508219.1:p.Ile2345Asn
|
|
NM_003126.3:c.7052T>A
|
NP_003117.2:p.Ile2351Asn
|
|
XM_011509916.2:c.7052T>A
|
XP_011508218.1:p.Ile2351Asn
|
|
XM_011509917.3:c.7034T>A
|
XP_011508219.1:p.Ile2345Asn
|
|
NM_003126.4:c.7052T>A
MANE Select
|
NP_003117.2:p.Ile2351Asn
|
|