ENST00000625662.3:c.2104C>G
|
|
|
ENST00000628118.2:c.1631C>G
|
|
|
ENST00000700551.1:c.*1428C>G
|
ENSP00000515057.1:n.*1428C>G
|
|
ENST00000394196.9:c.2597C>G
MANE Select
|
ENSP00000377747.4:p.Ser866Trp
|
|
ENST00000635856.1:n.3169C>G
|
|
|
ENST00000636306.1:n.157C>G
|
|
|
ENST00000636881.1:c.1968C>G
|
|
|
ENST00000637572.1:n.3341C>G
|
|
|
ENST00000394196.8:c.2597C>G
|
ENSP00000377747.4:p.Ser866Trp
|
|
ENST00000625463.1:c.137C>G
|
ENSP00000486391.1:p.Ser46Trp
|
|
ENST00000626874.2:c.2597C>G
|
ENSP00000486629.1:p.Ser866Trp
|
|
ENST00000628118.1:n.376C>G
|
|
|
NM_001271.3:c.2597C>G
|
NP_001262.3:p.Ser866Trp
|
|
NM_001271.4:c.2597C>G
MANE Select
|
NP_001262.3:p.Ser866Trp
|
|