ENST00000350026.11:c.4982A=
|
ENSP00000055163.8:p.Gln1661=
|
|
ENST00000414678.8:c.5051A=
|
ENSP00000412835.3:p.Gln1684=
|
|
ENST00000637015.2:c.5270A=
|
ENSP00000489729.2:p.Gln1757=
|
|
ENST00000346085.10:c.5021A=
|
ENSP00000344546.5:p.Gln1674=
|
|
ENST00000350026.10:c.4733A=
|
ENSP00000055163.7:p.Gln1578=
|
|
ENST00000414678.7:c.3299A=
|
ENSP00000412835.2:p.Gln1100=
|
|
ENST00000635849.1:c.2462A=
|
ENSP00000490948.1:p.Gln821=
|
|
ENST00000635957.1:c.2093A=
|
ENSP00000490385.1:p.Gln698=
|
|
ENST00000636227.1:n.3604A=
|
|
|
ENST00000636254.1:n.1061A=
|
|
|
ENST00000636930.2:c.5141A=
MANE Select
|
ENSP00000490491.2:p.Gln1714=
|
|
ENST00000636940.1:n.3138A=
|
|
|
ENST00000637015.1:c.2509A=
|
|
|
ENST00000637568.1:c.2423A=
|
|
|
ENST00000637741.1:n.1807A=
|
|
|
ENST00000637810.1:c.2483A=
|
ENSP00000489636.1:p.Gln828=
|
|
ENST00000637904.1:c.2642A=
|
ENSP00000490550.1:p.Gln881=
|
|
ENST00000647938.1:c.4772A=
|
ENSP00000498155.1:p.Gln1591=
|
|
ENST00000346085.9:c.4772A=
|
ENSP00000344546.4:p.Gln1591=
|
|
ENST00000350026.9:c.4733A=
|
ENSP00000055163.7:p.Gln1578=
|
|
ENST00000414678.6:c.3299A=
|
ENSP00000412835.2:p.Gln1100=
|
|
NM_017519.2:c.4733A=
|
NP_059989.2:p.Gln1578=
|
|
NM_020732.3:c.4772A=
|
NP_065783.3:p.Gln1591=
|
|
XM_005267069.3:c.4892A=
|
XP_005267126.2:p.Gln1631=
|
|
XM_011535984.1:c.3971A=
|
XP_011534286.1:p.Gln1324=
|
|
XM_011535985.1:c.3791A=
|
XP_011534287.1:p.Gln1264=
|
|
XM_011535986.1:c.3551A=
|
XP_011534288.1:p.Gln1184=
|
|
XM_011535987.1:c.3170A=
|
XP_011534289.1:p.Gln1057=
|
|
XM_011535988.1:c.2033A=
|
XP_011534290.1:p.Gln678=
|
|
NM_001346813.1:c.4892A=
|
NP_001333742.1:p.Gln1631=
|
|
NM_001363725.1:c.2642A=
|
NP_001350654.1:p.Gln881=
|
|
XM_011535984.2:c.5102A=
|
XP_011534286.2:p.Gln1701=
|
|
XM_011535988.3:c.2033A=
|
XP_011534290.1:p.Gln678=
|
|
XM_017011103.2:c.5003A=
|
XP_016866592.1:p.Gln1668=
|
|
XM_017011104.1:c.4973A=
|
XP_016866593.1:p.Gln1658=
|
|
XM_017011105.2:c.4943A=
|
XP_016866594.1:p.Gln1648=
|
|
XM_017011106.2:c.4814A=
|
XP_016866595.1:p.Gln1605=
|
|
XM_017011107.2:c.4793A=
|
XP_016866596.1:p.Gln1598=
|
|
XR_002956289.1:n.5088A=
|
|
|
NM_001363725.2:c.2642A=
|
NP_001350654.1:p.Gln881=
|
|
NM_001371656.1:c.5021A=
|
NP_001358585.1:p.Gln1674=
|
|
NM_001374820.1:c.5021A=
|
NP_001361749.1:p.Gln1674=
|
|
NM_001374828.1:c.5141A=
MANE Select
|
NP_001361757.1:p.Gln1714=
|
|
NM_017519.3:c.4982A=
|
NP_059989.3:p.Gln1661=
|
|