ENST00000394867.9:n.1554C>A
|
|
|
ENST00000688002.1:n.3266C>A
|
|
|
ENST00000688751.1:n.251C>A
|
|
|
ENST00000689792.1:n.1019C>A
|
|
|
ENST00000262948.10:c.1115C>A
MANE Select
|
ENSP00000262948.4:p.Ser372Tyr
|
|
ENST00000262948.9:c.1115C>A
|
ENSP00000262948.3:p.Ser372Tyr
|
|
ENST00000394867.8:c.824C>A
|
ENSP00000378336.1:p.Ser275Tyr
|
|
ENST00000597263.5:n.300C>A
|
|
|
ENST00000599021.1:c.225C>A
|
|
|
ENST00000600584.5:n.2564C>A
|
|
|
ENST00000601786.5:n.1416C>A
|
|
|
NM_030662.3:c.1115C>A , LRG_750t1:c.1115C>A
|
NP_109587.1:p.Ser372Tyr
|
|
XM_006722799.2:c.836C>A
|
XP_006722862.1:p.Ser279Tyr
|
|
XM_011528133.1:c.545C>A
|
XP_011526435.1:p.Ser182Tyr
|
|
NM_030662.4:c.1115C>A
MANE Select
|
NP_109587.1:p.Ser372Tyr
|
|