ENST00000350026.11:c.4892G>A
|
ENSP00000055163.8:p.Arg1631His
|
|
ENST00000414678.8:c.4961G>A
|
ENSP00000412835.3:p.Arg1654His
|
|
ENST00000637015.2:c.5180G>A
|
ENSP00000489729.2:p.Arg1727His
|
|
ENST00000346085.10:c.4931G>A
|
ENSP00000344546.5:p.Arg1644His
|
|
ENST00000350026.10:c.4643G>A
|
ENSP00000055163.7:p.Arg1548His
|
|
ENST00000414678.7:c.3209G>A
|
ENSP00000412835.2:p.Arg1070His
|
|
ENST00000635849.1:c.2372G>A
|
ENSP00000490948.1:p.Arg791His
|
|
ENST00000635957.1:c.2003G>A
|
ENSP00000490385.1:p.Arg668His
|
|
ENST00000636227.1:n.3514G>A
|
|
|
ENST00000636254.1:n.971G>A
|
|
|
ENST00000636930.2:c.5051G>A
MANE Select
|
ENSP00000490491.2:p.Arg1684His
|
|
ENST00000636940.1:n.3048G>A
|
|
|
ENST00000637015.1:c.2419G>A
|
|
|
ENST00000637568.1:c.2333G>A
|
|
|
ENST00000637741.1:n.1717G>A
|
|
|
ENST00000637810.1:c.2393G>A
|
ENSP00000489636.1:p.Arg798His
|
|
ENST00000637904.1:c.2552G>A
|
ENSP00000490550.1:p.Arg851His
|
|
ENST00000647938.1:c.4682G>A
|
ENSP00000498155.1:p.Arg1561His
|
|
ENST00000346085.9:c.4682G>A
|
ENSP00000344546.4:p.Arg1561His
|
|
ENST00000350026.9:c.4643G>A
|
ENSP00000055163.7:p.Arg1548His
|
|
ENST00000414678.6:c.3209G>A
|
ENSP00000412835.2:p.Arg1070His
|
|
NM_017519.2:c.4643G>A
|
NP_059989.2:p.Arg1548His
|
|
NM_020732.3:c.4682G>A
|
NP_065783.3:p.Arg1561His
|
|
XM_005267069.3:c.4802G>A
|
XP_005267126.2:p.Arg1601His
|
|
XM_011535984.1:c.3881G>A
|
XP_011534286.1:p.Arg1294His
|
|
XM_011535985.1:c.3701G>A
|
XP_011534287.1:p.Arg1234His
|
|
XM_011535986.1:c.3461G>A
|
XP_011534288.1:p.Arg1154His
|
|
XM_011535987.1:c.3080G>A
|
XP_011534289.1:p.Arg1027His
|
|
XM_011535988.1:c.1943G>A
|
XP_011534290.1:p.Arg648His
|
|
NM_001346813.1:c.4802G>A
|
NP_001333742.1:p.Arg1601His
|
|
NM_001363725.1:c.2552G>A
|
NP_001350654.1:p.Arg851His
|
|
XM_011535984.2:c.5012G>A
|
XP_011534286.2:p.Arg1671His
|
|
XM_011535988.3:c.1943G>A
|
XP_011534290.1:p.Arg648His
|
|
XM_017011103.2:c.4913G>A
|
XP_016866592.1:p.Arg1638His
|
|
XM_017011104.1:c.4883G>A
|
XP_016866593.1:p.Arg1628His
|
|
XM_017011105.2:c.4853G>A
|
XP_016866594.1:p.Arg1618His
|
|
XM_017011106.2:c.4724G>A
|
XP_016866595.1:p.Arg1575His
|
|
XM_017011107.2:c.4703G>A
|
XP_016866596.1:p.Arg1568His
|
|
XR_002956289.1:n.4998G>A
|
|
|
NM_001363725.2:c.2552G>A
|
NP_001350654.1:p.Arg851His
|
|
NM_001371656.1:c.4931G>A
|
NP_001358585.1:p.Arg1644His
|
|
NM_001374820.1:c.4931G>A
|
NP_001361749.1:p.Arg1644His
|
|
NM_001374828.1:c.5051G>A
MANE Select
|
NP_001361757.1:p.Arg1684His
|
|
NM_017519.3:c.4892G>A
|
NP_059989.3:p.Arg1631His
|
|