ENST00000350026.11:c.4647G>T
|
ENSP00000055163.8:p.Gln1549His
|
|
ENST00000414678.8:c.4716G>T
|
ENSP00000412835.3:p.Gln1572His
|
|
ENST00000637015.2:c.4935G>T
|
ENSP00000489729.2:p.Gln1645His
|
|
ENST00000346085.10:c.4686G>T
|
ENSP00000344546.5:p.Gln1562His
|
|
ENST00000350026.10:c.4398G>T
|
ENSP00000055163.7:p.Gln1466His
|
|
ENST00000414678.7:c.2964G>T
|
ENSP00000412835.2:p.Gln988His
|
|
ENST00000635849.1:c.2127G>T
|
ENSP00000490948.1:p.Gln709His
|
|
ENST00000635957.1:c.1758G>T
|
ENSP00000490385.1:p.Gln586His
|
|
ENST00000636227.1:n.3269G>T
|
|
|
ENST00000636254.1:n.726G>T
|
|
|
ENST00000636930.2:c.4806G>T
MANE Select
|
ENSP00000490491.2:p.Gln1602His
|
|
ENST00000636940.1:n.2803G>T
|
|
|
ENST00000637015.1:c.2174G>T
|
|
|
ENST00000637568.1:c.2088G>T
|
|
|
ENST00000637741.1:n.1472G>T
|
|
|
ENST00000637810.1:c.2148G>T
|
ENSP00000489636.1:p.Gln716His
|
|
ENST00000637904.1:c.2307G>T
|
ENSP00000490550.1:p.Gln769His
|
|
ENST00000647938.1:c.4437G>T
|
ENSP00000498155.1:p.Gln1479His
|
|
ENST00000346085.9:c.4437G>T
|
ENSP00000344546.4:p.Gln1479His
|
|
ENST00000350026.9:c.4398G>T
|
ENSP00000055163.7:p.Gln1466His
|
|
ENST00000414678.6:c.2964G>T
|
ENSP00000412835.2:p.Gln988His
|
|
NM_017519.2:c.4398G>T
|
NP_059989.2:p.Gln1466His
|
|
NM_020732.3:c.4437G>T
|
NP_065783.3:p.Gln1479His
|
|
XM_005267069.3:c.4557G>T
|
XP_005267126.2:p.Gln1519His
|
|
XM_011535984.1:c.3636G>T
|
XP_011534286.1:p.Gln1212His
|
|
XM_011535985.1:c.3456G>T
|
XP_011534287.1:p.Gln1152His
|
|
XM_011535986.1:c.3216G>T
|
XP_011534288.1:p.Gln1072His
|
|
XM_011535987.1:c.2835G>T
|
XP_011534289.1:p.Gln945His
|
|
XM_011535988.1:c.1698G>T
|
XP_011534290.1:p.Gln566His
|
|
NM_001346813.1:c.4557G>T
|
NP_001333742.1:p.Gln1519His
|
|
NM_001363725.1:c.2307G>T
|
NP_001350654.1:p.Gln769His
|
|
XM_011535984.2:c.4767G>T
|
XP_011534286.2:p.Gln1589His
|
|
XM_011535988.3:c.1698G>T
|
XP_011534290.1:p.Gln566His
|
|
XM_017011103.2:c.4668G>T
|
XP_016866592.1:p.Gln1556His
|
|
XM_017011104.1:c.4638G>T
|
XP_016866593.1:p.Gln1546His
|
|
XM_017011105.2:c.4608G>T
|
XP_016866594.1:p.Gln1536His
|
|
XM_017011106.2:c.4479G>T
|
XP_016866595.1:p.Gln1493His
|
|
XM_017011107.2:c.4458G>T
|
XP_016866596.1:p.Gln1486His
|
|
XR_002956289.1:n.4753G>T
|
|
|
NM_001363725.2:c.2307G>T
|
NP_001350654.1:p.Gln769His
|
|
NM_001371656.1:c.4686G>T
|
NP_001358585.1:p.Gln1562His
|
|
NM_001374820.1:c.4686G>T
|
NP_001361749.1:p.Gln1562His
|
|
NM_001374828.1:c.4806G>T
MANE Select
|
NP_001361757.1:p.Gln1602His
|
|
NM_017519.3:c.4647G>T
|
NP_059989.3:p.Gln1549His
|
|