ENST00000394867.9:n.1622C>T
|
|
|
ENST00000688002.1:n.3334C>T
|
|
|
ENST00000688751.1:n.319C>T
|
|
|
ENST00000689792.1:n.1087C>T
|
|
|
ENST00000262948.10:c.1183C>T
MANE Select
|
ENSP00000262948.4:p.Pro395Ser
|
|
ENST00000262948.9:c.1183C>T
|
ENSP00000262948.3:p.Pro395Ser
|
|
ENST00000394867.8:c.892C>T
|
ENSP00000378336.1:p.Pro298Ser
|
|
ENST00000597263.5:n.368C>T
|
|
|
ENST00000599021.1:c.293C>T
|
|
|
ENST00000600584.5:n.2632C>T
|
|
|
ENST00000601786.5:n.1484C>T
|
|
|
NM_030662.3:c.1183C>T , LRG_750t1:c.1183C>T
|
NP_109587.1:p.Pro395Ser
|
|
XM_006722799.2:c.904C>T
|
XP_006722862.1:p.Pro302Ser
|
|
XM_011528133.1:c.613C>T
|
XP_011526435.1:p.Pro205Ser
|
|
NM_030662.4:c.1183C>T
MANE Select
|
NP_109587.1:p.Pro395Ser
|
|