ENST00000255078.8:c.2073A>C
MANE Select
|
ENSP00000255078.4:p.Arg691Ser
|
|
ENST00000674675.1:c.317A>C
|
|
|
ENST00000674878.1:c.317A>C
|
|
|
ENST00000674955.1:c.*790A>C
|
ENSP00000502463.1:n.*790A>C
|
|
ENST00000675118.1:c.1561A>C
|
|
|
ENST00000675389.1:n.348A>C
|
|
|
ENST00000675615.1:c.2073A>C
|
ENSP00000502413.1:p.Arg691Ser
|
|
ENST00000675648.1:n.1448A>C
|
|
|
ENST00000675916.1:c.317A>C
|
|
|
ENST00000676173.1:n.2818A>C
|
|
|
ENST00000676182.1:c.504A>C
|
|
|
ENST00000676228.1:c.*1396A>C
|
ENSP00000502375.1:n.*1396A>C
|
|
ENST00000255078.7:c.2073A>C
|
ENSP00000255078.3:p.Arg691Ser
|
|
ENST00000539064.5:n.1832A>C
|
|
|
ENST00000543739.5:n.1066A>C
|
|
|
NM_002180.2:c.2073A>C , LRG_250t1:c.2073A>C
|
NP_002171.2:p.Arg691Ser
|
|
XM_005273974.2:c.1062A>C
|
XP_005274031.1:p.Arg354Ser
|
|
XM_005273975.2:c.945A>C
|
XP_005274032.1:p.Arg315Ser
|
|
XM_011544994.1:c.840A>C
|
XP_011543296.1:p.Arg280Ser
|
|
XR_949903.1:n.2175A>C
|
|
|
XM_005273975.3:c.945A>C
|
XP_005274032.1:p.Arg315Ser
|
|
XM_017017669.2:c.1062A>C
|
XP_016873158.1:p.Arg354Ser
|
|
XM_017017670.2:c.1062A>C
|
XP_016873159.1:p.Arg354Ser
|
|
XR_949903.3:n.2171A>C
|
|
|
NM_002180.3:c.2073A>C
MANE Select
|
NP_002171.2:p.Arg691Ser
|
|