ENST00000255078.8:c.1797G>C
MANE Select
|
ENSP00000255078.4:p.Val599=
|
|
ENST00000674675.1:c.41G>C
|
|
|
ENST00000674878.1:c.41G>C
|
|
|
ENST00000674955.1:c.*514G>C
|
ENSP00000502463.1:n.*514G>C
|
|
ENST00000675118.1:c.1285G>C
|
|
|
ENST00000675389.1:n.72G>C
|
|
|
ENST00000675615.1:c.1797G>C
|
ENSP00000502413.1:p.Val599=
|
|
ENST00000675648.1:n.1172G>C
|
|
|
ENST00000675916.1:c.41G>C
|
|
|
ENST00000676173.1:n.2542G>C
|
|
|
ENST00000676182.1:c.228G>C
|
|
|
ENST00000676228.1:c.*1120G>C
|
ENSP00000502375.1:n.*1120G>C
|
|
ENST00000255078.7:c.1797G>C
|
ENSP00000255078.3:p.Val599=
|
|
ENST00000539064.5:n.1556G>C
|
|
|
ENST00000541229.5:n.492G>C
|
|
|
ENST00000543739.5:n.790G>C
|
|
|
ENST00000545475.1:n.393G>C
|
|
|
NM_002180.2:c.1797G>C , LRG_250t1:c.1797G>C
|
NP_002171.2:p.Val599=
|
|
XM_005273974.2:c.786G>C
|
XP_005274031.1:p.Val262=
|
|
XM_005273975.2:c.669G>C
|
XP_005274032.1:p.Val223=
|
|
XM_011544994.1:c.564G>C
|
XP_011543296.1:p.Val188=
|
|
XR_949903.1:n.1899G>C
|
|
|
XM_005273975.3:c.669G>C
|
XP_005274032.1:p.Val223=
|
|
XM_017017669.2:c.786G>C
|
XP_016873158.1:p.Val262=
|
|
XM_017017670.2:c.786G>C
|
XP_016873159.1:p.Val262=
|
|
XR_949903.3:n.1895G>C
|
|
|
NM_002180.3:c.1797G>C
MANE Select
|
NP_002171.2:p.Val599=
|
|