ENST00000350026.11:c.4596G>T
|
ENSP00000055163.8:p.Gln1532His
|
|
ENST00000414678.8:c.4665G>T
|
ENSP00000412835.3:p.Gln1555His
|
|
ENST00000637015.2:c.4884G>T
|
ENSP00000489729.2:p.Gln1628His
|
|
ENST00000346085.10:c.4635G>T
|
ENSP00000344546.5:p.Gln1545His
|
|
ENST00000350026.10:c.4347G>T
|
ENSP00000055163.7:p.Gln1449His
|
|
ENST00000414678.7:c.2913G>T
|
ENSP00000412835.2:p.Gln971His
|
|
ENST00000635849.1:c.2076G>T
|
ENSP00000490948.1:p.Gln692His
|
|
ENST00000635957.1:c.1707G>T
|
ENSP00000490385.1:p.Gln569His
|
|
ENST00000636227.1:n.3218G>T
|
|
|
ENST00000636254.1:n.675G>T
|
|
|
ENST00000636930.2:c.4755G>T
MANE Select
|
ENSP00000490491.2:p.Gln1585His
|
|
ENST00000636940.1:n.2752G>T
|
|
|
ENST00000637015.1:c.2123G>T
|
|
|
ENST00000637568.1:c.2037G>T
|
|
|
ENST00000637741.1:n.1421G>T
|
|
|
ENST00000637810.1:c.2097G>T
|
ENSP00000489636.1:p.Gln699His
|
|
ENST00000637904.1:c.2256G>T
|
ENSP00000490550.1:p.Gln752His
|
|
ENST00000647938.1:c.4386G>T
|
ENSP00000498155.1:p.Gln1462His
|
|
ENST00000346085.9:c.4386G>T
|
ENSP00000344546.4:p.Gln1462His
|
|
ENST00000350026.9:c.4347G>T
|
ENSP00000055163.7:p.Gln1449His
|
|
ENST00000414678.6:c.2913G>T
|
ENSP00000412835.2:p.Gln971His
|
|
NM_017519.2:c.4347G>T
|
NP_059989.2:p.Gln1449His
|
|
NM_020732.3:c.4386G>T
|
NP_065783.3:p.Gln1462His
|
|
XM_005267069.3:c.4506G>T
|
XP_005267126.2:p.Gln1502His
|
|
XM_011535984.1:c.3585G>T
|
XP_011534286.1:p.Gln1195His
|
|
XM_011535985.1:c.3405G>T
|
XP_011534287.1:p.Gln1135His
|
|
XM_011535986.1:c.3165G>T
|
XP_011534288.1:p.Gln1055His
|
|
XM_011535987.1:c.2784G>T
|
XP_011534289.1:p.Gln928His
|
|
XM_011535988.1:c.1647G>T
|
XP_011534290.1:p.Gln549His
|
|
NM_001346813.1:c.4506G>T
|
NP_001333742.1:p.Gln1502His
|
|
NM_001363725.1:c.2256G>T
|
NP_001350654.1:p.Gln752His
|
|
XM_011535984.2:c.4716G>T
|
XP_011534286.2:p.Gln1572His
|
|
XM_011535988.3:c.1647G>T
|
XP_011534290.1:p.Gln549His
|
|
XM_017011103.2:c.4617G>T
|
XP_016866592.1:p.Gln1539His
|
|
XM_017011104.1:c.4587G>T
|
XP_016866593.1:p.Gln1529His
|
|
XM_017011105.2:c.4557G>T
|
XP_016866594.1:p.Gln1519His
|
|
XM_017011106.2:c.4428G>T
|
XP_016866595.1:p.Gln1476His
|
|
XM_017011107.2:c.4407G>T
|
XP_016866596.1:p.Gln1469His
|
|
XR_002956289.1:n.4702G>T
|
|
|
NM_001363725.2:c.2256G>T
|
NP_001350654.1:p.Gln752His
|
|
NM_001371656.1:c.4635G>T
|
NP_001358585.1:p.Gln1545His
|
|
NM_001374820.1:c.4635G>T
|
NP_001361749.1:p.Gln1545His
|
|
NM_001374828.1:c.4755G>T
MANE Select
|
NP_001361757.1:p.Gln1585His
|
|
NM_017519.3:c.4596G>T
|
NP_059989.3:p.Gln1532His
|
|