ENST00000350026.11:c.3063G>T
|
ENSP00000055163.8:p.Gln1021His
|
|
ENST00000414678.8:c.2973G>T
|
ENSP00000412835.3:p.Gln991His
|
|
ENST00000637015.2:c.3063G>T
|
ENSP00000489729.2:p.Gln1021His
|
|
ENST00000319584.11:c.1077G>T
|
ENSP00000313006.7:p.Gln359His
|
|
ENST00000346085.10:c.3102G>T
|
ENSP00000344546.5:p.Gln1034His
|
|
ENST00000350026.10:c.2814G>T
|
ENSP00000055163.7:p.Gln938His
|
|
ENST00000414678.7:c.1221G>T
|
ENSP00000412835.2:p.Gln407His
|
|
ENST00000452544.2:n.964G>T
|
|
|
ENST00000635849.1:c.384G>T
|
ENSP00000490948.1:p.Gln128His
|
|
ENST00000635957.1:c.18G>T
|
ENSP00000490385.1:p.Gln6His
|
|
ENST00000636426.1:n.197G>T
|
|
|
ENST00000636930.2:c.3063G>T
MANE Select
|
ENSP00000490491.2:p.Gln1021His
|
|
ENST00000637015.1:c.302G>T
|
|
|
ENST00000637568.1:c.106G>T
|
|
|
ENST00000637810.1:c.564G>T
|
ENSP00000489636.1:p.Gln188His
|
|
ENST00000637904.1:c.564G>T
|
ENSP00000490550.1:p.Gln188His
|
|
ENST00000647938.1:c.2853G>T
|
ENSP00000498155.1:p.Gln951His
|
|
ENST00000674190.1:n.1812G>T
|
|
|
ENST00000319584.10:c.1080G>T
|
ENSP00000313006.6:p.Gln360His
|
|
ENST00000346085.9:c.2853G>T
|
ENSP00000344546.4:p.Gln951His
|
|
ENST00000350026.9:c.2814G>T
|
ENSP00000055163.7:p.Gln938His
|
|
ENST00000400790.3:c.15G>T
|
ENSP00000383596.3:p.Gln5His
|
|
ENST00000414678.6:c.1221G>T
|
ENSP00000412835.2:p.Gln407His
|
|
ENST00000452544.1:n.910G>T
|
|
|
ENST00000478761.3:c.136G>T
|
|
|
NM_017519.2:c.2814G>T
|
NP_059989.2:p.Gln938His
|
|
NM_020732.3:c.2853G>T
|
NP_065783.3:p.Gln951His
|
|
XM_005267069.3:c.2814G>T
|
XP_005267126.2:p.Gln938His
|
|
XM_011535984.1:c.1764G>T
|
XP_011534286.1:p.Gln588His
|
|
XM_011535985.1:c.1584G>T
|
XP_011534287.1:p.Gln528His
|
|
XM_011535986.1:c.1344G>T
|
XP_011534288.1:p.Gln448His
|
|
XM_011535987.1:c.963G>T
|
XP_011534289.1:p.Gln321His
|
|
XM_011535988.1:c.-20+15718G>T
|
XP_011534290.1:n.-20+15718G>T
|
|
NM_001346813.1:c.2814G>T
|
NP_001333742.1:p.Gln938His
|
|
NM_001363725.1:c.564G>T
|
NP_001350654.1:p.Gln188His
|
|
XM_011535984.2:c.2895G>T
|
XP_011534286.2:p.Gln965His
|
|
XM_011535988.3:c.-20+15718G>T
|
XP_011534290.1:n.-20+15718G>T
|
|
XM_017011103.2:c.2895G>T
|
XP_016866592.1:p.Gln965His
|
|
XM_017011104.1:c.2895G>T
|
XP_016866593.1:p.Gln965His
|
|
XM_017011105.2:c.2895G>T
|
XP_016866594.1:p.Gln965His
|
|
XM_017011106.2:c.2895G>T
|
XP_016866595.1:p.Gln965His
|
|
XM_017011107.2:c.2715G>T
|
XP_016866596.1:p.Gln905His
|
|
XR_002956289.1:n.2978G>T
|
|
|
NM_001363725.2:c.564G>T
|
NP_001350654.1:p.Gln188His
|
|
NM_001371656.1:c.3102G>T
|
NP_001358585.1:p.Gln1034His
|
|
NM_001374820.1:c.3102G>T
|
NP_001361749.1:p.Gln1034His
|
|
NM_001374828.1:c.3063G>T
MANE Select
|
NP_001361757.1:p.Gln1021His
|
|
NM_017519.3:c.3063G>T
|
NP_059989.3:p.Gln1021His
|
|