ENST00000255078.8:c.2256C>A
MANE Select
|
ENSP00000255078.4:p.Ser752=
|
|
ENST00000674675.1:c.500C>A
|
|
|
ENST00000674878.1:c.500C>A
|
|
|
ENST00000674955.1:c.*973C>A
|
ENSP00000502463.1:n.*973C>A
|
|
ENST00000675118.1:c.1744C>A
|
|
|
ENST00000675389.1:n.531C>A
|
|
|
ENST00000675615.1:c.2256C>A
|
ENSP00000502413.1:p.Ser752=
|
|
ENST00000675648.1:n.1631C>A
|
|
|
ENST00000675916.1:c.500C>A
|
|
|
ENST00000676173.1:n.3001C>A
|
|
|
ENST00000676182.1:c.687C>A
|
|
|
ENST00000676228.1:c.*1579C>A
|
ENSP00000502375.1:n.*1579C>A
|
|
ENST00000255078.7:c.2256C>A
|
ENSP00000255078.3:p.Ser752=
|
|
ENST00000539064.5:n.2015C>A
|
|
|
ENST00000543739.5:n.1249C>A
|
|
|
NM_002180.2:c.2256C>A , LRG_250t1:c.2256C>A
|
NP_002171.2:p.Ser752=
|
|
XM_005273974.2:c.1245C>A
|
XP_005274031.1:p.Ser415=
|
|
XM_005273975.2:c.1128C>A
|
XP_005274032.1:p.Ser376=
|
|
XM_011544994.1:c.1023C>A
|
XP_011543296.1:p.Ser341=
|
|
XR_949903.1:n.2358C>A
|
|
|
XM_005273975.3:c.1128C>A
|
XP_005274032.1:p.Ser376=
|
|
XM_017017669.2:c.1245C>A
|
XP_016873158.1:p.Ser415=
|
|
XM_017017670.2:c.1245C>A
|
XP_016873159.1:p.Ser415=
|
|
XR_949903.3:n.2354C>A
|
|
|
NM_002180.3:c.2256C>A
MANE Select
|
NP_002171.2:p.Ser752=
|
|