ENST00000350026.11:c.2790T>A
|
ENSP00000055163.8:p.Ser930Arg
|
|
ENST00000414678.8:c.2700T>A
|
ENSP00000412835.3:p.Ser900Arg
|
|
ENST00000637015.2:c.2790T>A
|
ENSP00000489729.2:p.Ser930Arg
|
|
ENST00000319584.11:c.804T>A
|
ENSP00000313006.7:p.Ser268Arg
|
|
ENST00000346085.10:c.2829T>A
|
ENSP00000344546.5:p.Ser943Arg
|
|
ENST00000350026.10:c.2541T>A
|
ENSP00000055163.7:p.Ser847Arg
|
|
ENST00000414678.7:c.948T>A
|
ENSP00000412835.2:p.Ser316Arg
|
|
ENST00000452544.2:n.691T>A
|
|
|
ENST00000635849.1:c.111T>A
|
ENSP00000490948.1:p.Ser37Arg
|
|
ENST00000636930.2:c.2790T>A
MANE Select
|
ENSP00000490491.2:p.Ser930Arg
|
|
ENST00000637015.1:c.29T>A
|
|
|
ENST00000637810.1:c.291T>A
|
ENSP00000489636.1:p.Ser97Arg
|
|
ENST00000637904.1:c.291T>A
|
ENSP00000490550.1:p.Ser97Arg
|
|
ENST00000647938.1:c.2580T>A
|
ENSP00000498155.1:p.Ser860Arg
|
|
ENST00000674190.1:n.1539T>A
|
|
|
ENST00000319584.10:c.807T>A
|
ENSP00000313006.6:p.Ser269Arg
|
|
ENST00000346085.9:c.2580T>A
|
ENSP00000344546.4:p.Ser860Arg
|
|
ENST00000350026.9:c.2541T>A
|
ENSP00000055163.7:p.Ser847Arg
|
|
ENST00000414678.6:c.948T>A
|
ENSP00000412835.2:p.Ser316Arg
|
|
ENST00000452544.1:n.637T>A
|
|
|
NM_017519.2:c.2541T>A
|
NP_059989.2:p.Ser847Arg
|
|
NM_020732.3:c.2580T>A
|
NP_065783.3:p.Ser860Arg
|
|
XM_005267069.3:c.2541T>A
|
XP_005267126.2:p.Ser847Arg
|
|
XM_011535984.1:c.1491T>A
|
XP_011534286.1:p.Ser497Arg
|
|
XM_011535985.1:c.1311T>A
|
XP_011534287.1:p.Ser437Arg
|
|
XM_011535986.1:c.1071T>A
|
XP_011534288.1:p.Ser357Arg
|
|
XM_011535987.1:c.690T>A
|
XP_011534289.1:p.Ser230Arg
|
|
XM_011535988.1:c.-20+15445T>A
|
XP_011534290.1:n.-20+15445T>A
|
|
NM_001346813.1:c.2541T>A
|
NP_001333742.1:p.Ser847Arg
|
|
NM_001363725.1:c.291T>A
|
NP_001350654.1:p.Ser97Arg
|
|
XM_011535984.2:c.2622T>A
|
XP_011534286.2:p.Ser874Arg
|
|
XM_011535988.3:c.-20+15445T>A
|
XP_011534290.1:n.-20+15445T>A
|
|
XM_017011103.2:c.2622T>A
|
XP_016866592.1:p.Ser874Arg
|
|
XM_017011104.1:c.2622T>A
|
XP_016866593.1:p.Ser874Arg
|
|
XM_017011105.2:c.2622T>A
|
XP_016866594.1:p.Ser874Arg
|
|
XM_017011106.2:c.2622T>A
|
XP_016866595.1:p.Ser874Arg
|
|
XM_017011107.2:c.2442T>A
|
XP_016866596.1:p.Ser814Arg
|
|
XR_002956289.1:n.2705T>A
|
|
|
NM_001363725.2:c.291T>A
|
NP_001350654.1:p.Ser97Arg
|
|
NM_001371656.1:c.2829T>A
|
NP_001358585.1:p.Ser943Arg
|
|
NM_001374820.1:c.2829T>A
|
NP_001361749.1:p.Ser943Arg
|
|
NM_001374828.1:c.2790T>A
MANE Select
|
NP_001361757.1:p.Ser930Arg
|
|
NM_017519.3:c.2790T>A
|
NP_059989.3:p.Ser930Arg
|
|