ENST00000683611.1:n.1119A>G
|
|
|
ENST00000265104.5:c.13786A>G
MANE Select
|
ENSP00000265104.4:p.Asn4596Asp
|
|
ENST00000681290.1:c.13741A>G
|
ENSP00000505288.1:p.Asn4581Asp
|
|
ENST00000265104.4:c.13786A>G
|
ENSP00000265104.4:p.Asn4596Asp
|
|
NM_001369.2:c.13786A>G
|
NP_001360.1:p.Asn4596Asp
|
|
XM_005248262.2:c.13741A>G
|
XP_005248319.1:p.Asn4581Asp
|
|
XM_005248262.3:c.13894A>G
|
XP_005248319.2:p.Asn4632Asp
|
|
XM_017009177.1:c.13474A>G
|
XP_016864666.1:p.Asn4492Asp
|
|
XM_017009178.1:c.12799A>G
|
XP_016864667.1:p.Asn4267Asp
|
|
XM_017009179.2:c.12799A>G
|
XP_016864668.1:p.Asn4267Asp
|
|
XM_017009185.1:c.8983A>G
|
XP_016864674.1:p.Asn2995Asp
|
|
XM_017009186.1:c.8536A>G
|
XP_016864675.1:p.Asn2846Asp
|
|
XM_017009188.1:c.7873A>G
|
XP_016864677.1:p.Asn2625Asp
|
|
XM_024454388.1:c.12799A>G
|
XP_024310156.1:p.Asn4267Asp
|
|
XM_024454389.1:c.12388A>G
|
XP_024310157.1:p.Asn4130Asp
|
|
NM_001369.3:c.13786A>G
MANE Select
|
NP_001360.1:p.Asn4596Asp
|
|