ENST00000302068.9:c.1218C>T
MANE Select
|
ENSP00000306099.4:p.Ser406=
|
|
ENST00000302068.8:c.1218C>T
|
ENSP00000306099.4:p.Ser406=
|
|
ENST00000502545.5:n.939+466C>T
|
|
|
ENST00000509493.1:c.561C>T
|
ENSP00000426757.1:p.Ser187=
|
|
NM_001184741.1:c.1041C>T
|
NP_001171670.1:p.Ser347=
|
|
NM_005141.4:c.1218C>T , LRG_558t1:c.1218C>T
|
NP_005132.2:p.Ser406=
|
|
NM_001382759.1:c.1086C>T
|
NP_001369688.1:p.Ser362=
|
|
NM_001382760.1:c.1218C>T
|
NP_001369689.1:p.Ser406=
|
|
NM_001382761.1:c.1218C>T
|
NP_001369690.1:p.Ser406=
|
|
NM_001382762.1:c.918C>T
|
NP_001369691.1:p.Ser306=
|
|
NM_001382763.1:c.1209C>T
|
NP_001369692.1:p.Ser403=
|
|
NM_001382764.1:c.1081C>T
|
NP_001369693.1:p.His361Tyr
|
|
NM_001382765.1:c.1218C>T
|
NP_001369694.1:p.Ser406=
|
|
NM_005141.5:c.1218C>T
MANE Select
|
NP_005132.2:p.Ser406=
|
|