ENST00000255078.8:c.2446G>C
MANE Select
|
ENSP00000255078.4:p.Glu816Gln
|
|
ENST00000674675.1:c.591G>C
|
|
|
ENST00000674878.1:c.551G>C
|
|
|
ENST00000675118.1:c.1934G>C
|
|
|
ENST00000675389.1:n.721G>C
|
|
|
ENST00000675615.1:c.2446G>C
|
ENSP00000502413.1:p.Glu816Gln
|
|
ENST00000675648.1:n.1821G>C
|
|
|
ENST00000675916.1:c.690G>C
|
|
|
ENST00000676173.1:n.3191G>C
|
|
|
ENST00000676182.1:c.877G>C
|
|
|
ENST00000676228.1:c.*1769G>C
|
ENSP00000502375.1:n.*1769G>C
|
|
ENST00000255078.7:c.2446G>C
|
ENSP00000255078.3:p.Glu816Gln
|
|
ENST00000539064.5:n.2205G>C
|
|
|
ENST00000543739.5:n.1439G>C
|
|
|
NM_002180.2:c.2446G>C , LRG_250t1:c.2446G>C
|
NP_002171.2:p.Glu816Gln
|
|
XM_005273974.2:c.1435G>C
|
XP_005274031.1:p.Glu479Gln
|
|
XM_005273975.2:c.1318G>C
|
XP_005274032.1:p.Glu440Gln
|
|
XM_011544994.1:c.1213G>C
|
XP_011543296.1:p.Glu405Gln
|
|
XR_949903.1:n.2548G>C
|
|
|
XM_005273975.3:c.1318G>C
|
XP_005274032.1:p.Glu440Gln
|
|
XM_017017669.2:c.1435G>C
|
XP_016873158.1:p.Glu479Gln
|
|
XM_017017670.2:c.1435G>C
|
XP_016873159.1:p.Glu479Gln
|
|
XR_949903.3:n.2544G>C
|
|
|
NM_002180.3:c.2446G>C
MANE Select
|
NP_002171.2:p.Glu816Gln
|
|