ENST00000350026.11:c.3920A>G
|
ENSP00000055163.8:p.His1307Arg
|
|
ENST00000414678.8:c.3989A>G
|
ENSP00000412835.3:p.His1330Arg
|
|
ENST00000637015.2:c.4208A>G
|
ENSP00000489729.2:p.His1403Arg
|
|
ENST00000346085.10:c.3959A>G
|
ENSP00000344546.5:p.His1320Arg
|
|
ENST00000350026.10:c.3671A>G
|
ENSP00000055163.7:p.His1224Arg
|
|
ENST00000414678.7:c.2237A>G
|
ENSP00000412835.2:p.His746Arg
|
|
ENST00000635849.1:c.1400A>G
|
ENSP00000490948.1:p.His467Arg
|
|
ENST00000635957.1:c.1031A>G
|
ENSP00000490385.1:p.His344Arg
|
|
ENST00000636930.2:c.4079A>G
MANE Select
|
ENSP00000490491.2:p.His1360Arg
|
|
ENST00000636940.1:n.2076A>G
|
|
|
ENST00000637015.1:c.1447A>G
|
|
|
ENST00000637568.1:c.1361A>G
|
|
|
ENST00000637741.1:n.745A>G
|
|
|
ENST00000637810.1:c.1421A>G
|
ENSP00000489636.1:p.His474Arg
|
|
ENST00000637904.1:c.1580A>G
|
ENSP00000490550.1:p.His527Arg
|
|
ENST00000647938.1:c.3710A>G
|
ENSP00000498155.1:p.His1237Arg
|
|
ENST00000346085.9:c.3710A>G
|
ENSP00000344546.4:p.His1237Arg
|
|
ENST00000350026.9:c.3671A>G
|
ENSP00000055163.7:p.His1224Arg
|
|
ENST00000414678.6:c.2237A>G
|
ENSP00000412835.2:p.His746Arg
|
|
NM_017519.2:c.3671A>G
|
NP_059989.2:p.His1224Arg
|
|
NM_020732.3:c.3710A>G
|
NP_065783.3:p.His1237Arg
|
|
XM_005267069.3:c.3830A>G
|
XP_005267126.2:p.His1277Arg
|
|
XM_011535984.1:c.2909A>G
|
XP_011534286.1:p.His970Arg
|
|
XM_011535985.1:c.2729A>G
|
XP_011534287.1:p.His910Arg
|
|
XM_011535986.1:c.2489A>G
|
XP_011534288.1:p.His830Arg
|
|
XM_011535987.1:c.2108A>G
|
XP_011534289.1:p.His703Arg
|
|
XM_011535988.1:c.971A>G
|
XP_011534290.1:p.His324Arg
|
|
NM_001346813.1:c.3830A>G
|
NP_001333742.1:p.His1277Arg
|
|
NM_001363725.1:c.1580A>G
|
NP_001350654.1:p.His527Arg
|
|
XM_011535984.2:c.4040A>G
|
XP_011534286.2:p.His1347Arg
|
|
XM_011535988.3:c.971A>G
|
XP_011534290.1:p.His324Arg
|
|
XM_017011103.2:c.3941A>G
|
XP_016866592.1:p.His1314Arg
|
|
XM_017011104.1:c.3911A>G
|
XP_016866593.1:p.His1304Arg
|
|
XM_017011105.2:c.3881A>G
|
XP_016866594.1:p.His1294Arg
|
|
XM_017011106.2:c.3752A>G
|
XP_016866595.1:p.His1251Arg
|
|
XM_017011107.2:c.3731A>G
|
XP_016866596.1:p.His1244Arg
|
|
XR_002956289.1:n.4123A>G
|
|
|
NM_001363725.2:c.1580A>G
|
NP_001350654.1:p.His527Arg
|
|
NM_001371656.1:c.3959A>G
|
NP_001358585.1:p.His1320Arg
|
|
NM_001374820.1:c.3959A>G
|
NP_001361749.1:p.His1320Arg
|
|
NM_001374828.1:c.4079A>G
MANE Select
|
NP_001361757.1:p.His1360Arg
|
|
NM_017519.3:c.3920A>G
|
NP_059989.3:p.His1307Arg
|
|