ENST00000302068.9:c.1181A>G
MANE Select
|
ENSP00000306099.4:p.Asn394Ser
|
|
ENST00000302068.8:c.1181A>G
|
ENSP00000306099.4:p.Asn394Ser
|
|
ENST00000502545.5:n.939+429A>G
|
|
|
ENST00000509493.1:c.524A>G
|
ENSP00000426757.1:p.Asn175Ser
|
|
NM_001184741.1:c.1004A>G
|
NP_001171670.1:p.Asn335Ser
|
|
NM_005141.4:c.1181A>G , LRG_558t1:c.1181A>G
|
NP_005132.2:p.Asn394Ser
|
|
NM_001382759.1:c.1049A>G
|
NP_001369688.1:p.Asn350Ser
|
|
NM_001382760.1:c.1181A>G
|
NP_001369689.1:p.Asn394Ser
|
|
NM_001382761.1:c.1181A>G
|
NP_001369690.1:p.Asn394Ser
|
|
NM_001382762.1:c.881A>G
|
NP_001369691.1:p.Asn294Ser
|
|
NM_001382763.1:c.1172A>G
|
NP_001369692.1:p.Asn391Ser
|
|
NM_001382764.1:c.1081-37A>G
|
NP_001369693.1:n.1081-37A>G
|
|
NM_001382765.1:c.1181A>G
|
NP_001369694.1:p.Asn394Ser
|
|
NM_005141.5:c.1181A>G
MANE Select
|
NP_005132.2:p.Asn394Ser
|
|