ENST00000350026.11:c.3434G>A
|
ENSP00000055163.8:p.Arg1145Gln
|
|
ENST00000414678.8:c.3503G>A
|
ENSP00000412835.3:p.Arg1168Gln
|
|
ENST00000637015.2:c.3722G>A
|
ENSP00000489729.2:p.Arg1241Gln
|
|
ENST00000319584.11:c.1607G>A
|
ENSP00000313006.7:p.Arg536Gln
|
|
ENST00000346085.10:c.3473G>A
|
ENSP00000344546.5:p.Arg1158Gln
|
|
ENST00000350026.10:c.3185G>A
|
ENSP00000055163.7:p.Arg1062Gln
|
|
ENST00000414678.7:c.1751G>A
|
ENSP00000412835.2:p.Arg584Gln
|
|
ENST00000635849.1:c.914G>A
|
ENSP00000490948.1:p.Arg305Gln
|
|
ENST00000635957.1:c.548G>A
|
ENSP00000490385.1:p.Arg183Gln
|
|
ENST00000636930.2:c.3593G>A
MANE Select
|
ENSP00000490491.2:p.Arg1198Gln
|
|
ENST00000636940.1:n.1590G>A
|
|
|
ENST00000637015.1:c.961G>A
|
|
|
ENST00000637568.1:c.875G>A
|
|
|
ENST00000637741.1:n.259G>A
|
|
|
ENST00000637810.1:c.935G>A
|
ENSP00000489636.1:p.Arg312Gln
|
|
ENST00000637904.1:c.1094G>A
|
ENSP00000490550.1:p.Arg365Gln
|
|
ENST00000647938.1:c.3224G>A
|
ENSP00000498155.1:p.Arg1075Gln
|
|
ENST00000319584.10:c.1610G>A
|
ENSP00000313006.6:p.Arg537Gln
|
|
ENST00000346085.9:c.3224G>A
|
ENSP00000344546.4:p.Arg1075Gln
|
|
ENST00000350026.9:c.3185G>A
|
ENSP00000055163.7:p.Arg1062Gln
|
|
ENST00000400790.3:c.386G>A
|
ENSP00000383596.3:p.Arg129Gln
|
|
ENST00000414678.6:c.1751G>A
|
ENSP00000412835.2:p.Arg584Gln
|
|
ENST00000478761.3:c.795G>A
|
|
|
NM_017519.2:c.3185G>A
|
NP_059989.2:p.Arg1062Gln
|
|
NM_020732.3:c.3224G>A
|
NP_065783.3:p.Arg1075Gln
|
|
XM_005267069.3:c.3344G>A
|
XP_005267126.2:p.Arg1115Gln
|
|
XM_011535984.1:c.2423G>A
|
XP_011534286.1:p.Arg808Gln
|
|
XM_011535985.1:c.2243G>A
|
XP_011534287.1:p.Arg748Gln
|
|
XM_011535986.1:c.2003G>A
|
XP_011534288.1:p.Arg668Gln
|
|
XM_011535987.1:c.1622G>A
|
XP_011534289.1:p.Arg541Gln
|
|
XM_011535988.1:c.485G>A
|
XP_011534290.1:p.Arg162Gln
|
|
NM_001346813.1:c.3344G>A
|
NP_001333742.1:p.Arg1115Gln
|
|
NM_001363725.1:c.1094G>A
|
NP_001350654.1:p.Arg365Gln
|
|
XM_011535984.2:c.3554G>A
|
XP_011534286.2:p.Arg1185Gln
|
|
XM_011535988.3:c.485G>A
|
XP_011534290.1:p.Arg162Gln
|
|
XM_017011103.2:c.3455G>A
|
XP_016866592.1:p.Arg1152Gln
|
|
XM_017011104.1:c.3425G>A
|
XP_016866593.1:p.Arg1142Gln
|
|
XM_017011105.2:c.3395G>A
|
XP_016866594.1:p.Arg1132Gln
|
|
XM_017011106.2:c.3266G>A
|
XP_016866595.1:p.Arg1089Gln
|
|
XM_017011107.2:c.3245G>A
|
XP_016866596.1:p.Arg1082Gln
|
|
XR_002956289.1:n.3637G>A
|
|
|
NM_001363725.2:c.1094G>A
|
NP_001350654.1:p.Arg365Gln
|
|
NM_001371656.1:c.3473G>A
|
NP_001358585.1:p.Arg1158Gln
|
|
NM_001374820.1:c.3473G>A
|
NP_001361749.1:p.Arg1158Gln
|
|
NM_001374828.1:c.3593G>A
MANE Select
|
NP_001361757.1:p.Arg1198Gln
|
|
NM_017519.3:c.3434G>A
|
NP_059989.3:p.Arg1145Gln
|
|