ENST00000255078.8:c.2383C>T
MANE Select
|
ENSP00000255078.4:p.Pro795Ser
|
|
ENST00000674675.1:c.587+40C>T
|
|
|
ENST00000674878.1:c.548-60C>T
|
|
|
ENST00000675118.1:c.1871C>T
|
|
|
ENST00000675389.1:n.658C>T
|
|
|
ENST00000675615.1:c.2383C>T
|
ENSP00000502413.1:p.Pro795Ser
|
|
ENST00000675648.1:n.1758C>T
|
|
|
ENST00000675916.1:c.627C>T
|
|
|
ENST00000676173.1:n.3128C>T
|
|
|
ENST00000676182.1:c.814C>T
|
|
|
ENST00000676228.1:c.*1706C>T
|
ENSP00000502375.1:n.*1706C>T
|
|
ENST00000255078.7:c.2383C>T
|
ENSP00000255078.3:p.Pro795Ser
|
|
ENST00000539064.5:n.2142C>T
|
|
|
ENST00000543739.5:n.1376C>T
|
|
|
NM_002180.2:c.2383C>T , LRG_250t1:c.2383C>T
|
NP_002171.2:p.Pro795Ser
|
|
XM_005273974.2:c.1372C>T
|
XP_005274031.1:p.Pro458Ser
|
|
XM_005273975.2:c.1255C>T
|
XP_005274032.1:p.Pro419Ser
|
|
XM_011544994.1:c.1150C>T
|
XP_011543296.1:p.Pro384Ser
|
|
XR_949903.1:n.2485C>T
|
|
|
XM_005273975.3:c.1255C>T
|
XP_005274032.1:p.Pro419Ser
|
|
XM_017017669.2:c.1372C>T
|
XP_016873158.1:p.Pro458Ser
|
|
XM_017017670.2:c.1372C>T
|
XP_016873159.1:p.Pro458Ser
|
|
XR_949903.3:n.2481C>T
|
|
|
NM_002180.3:c.2383C>T
MANE Select
|
NP_002171.2:p.Pro795Ser
|
|