ENST00000302068.9:c.1235A>G
MANE Select
|
ENSP00000306099.4:p.Asn412Ser
|
|
ENST00000302068.8:c.1235A>G
|
ENSP00000306099.4:p.Asn412Ser
|
|
ENST00000502545.5:n.939+483A>G
|
|
|
ENST00000509493.1:c.578A>G
|
ENSP00000426757.1:p.Asn193Ser
|
|
NM_001184741.1:c.1058A>G
|
NP_001171670.1:p.Asn353Ser
|
|
NM_005141.4:c.1235A>G , LRG_558t1:c.1235A>G
|
NP_005132.2:p.Asn412Ser
|
|
NM_001382759.1:c.1103A>G
|
NP_001369688.1:p.Asn368Ser
|
|
NM_001382760.1:c.1235A>G
|
NP_001369689.1:p.Asn412Ser
|
|
NM_001382761.1:c.1235A>G
|
NP_001369690.1:p.Asn412Ser
|
|
NM_001382762.1:c.935A>G
|
NP_001369691.1:p.Asn312Ser
|
|
NM_001382763.1:c.1226A>G
|
NP_001369692.1:p.Asn409Ser
|
|
NM_001382764.1:c.*9A>G
|
NP_001369693.1:n.*9A>G
|
|
NM_001382765.1:c.1220+15A>G
|
NP_001369694.1:n.1220+15A>G
|
|
NM_005141.5:c.1235A>G
MANE Select
|
NP_005132.2:p.Asn412Ser
|
|