ENST00000350026.11:c.4642A>C
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ENSP00000055163.8:p.Arg1548=
|
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ENST00000414678.8:c.4711A>C
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ENSP00000412835.3:p.Arg1571=
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ENST00000637015.2:c.4930A>C
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ENSP00000489729.2:p.Arg1644=
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ENST00000346085.10:c.4681A>C
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ENSP00000344546.5:p.Arg1561=
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ENST00000350026.10:c.4393A>C
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ENSP00000055163.7:p.Arg1465=
|
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ENST00000414678.7:c.2959A>C
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ENSP00000412835.2:p.Arg987=
|
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ENST00000635849.1:c.2122A>C
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ENSP00000490948.1:p.Arg708=
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ENST00000635957.1:c.1753A>C
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ENSP00000490385.1:p.Arg585=
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ENST00000636227.1:n.3264A>C
|
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ENST00000636254.1:n.721A>C
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ENST00000636930.2:c.4801A>C
MANE Select
|
ENSP00000490491.2:p.Arg1601=
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ENST00000636940.1:n.2798A>C
|
|
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ENST00000637015.1:c.2169A>C
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ENST00000637568.1:c.2083A>C
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ENST00000637741.1:n.1467A>C
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ENST00000637810.1:c.2143A>C
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ENSP00000489636.1:p.Arg715=
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ENST00000637904.1:c.2302A>C
|
ENSP00000490550.1:p.Arg768=
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ENST00000647938.1:c.4432A>C
|
ENSP00000498155.1:p.Arg1478=
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ENST00000346085.9:c.4432A>C
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ENSP00000344546.4:p.Arg1478=
|
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ENST00000350026.9:c.4393A>C
|
ENSP00000055163.7:p.Arg1465=
|
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ENST00000414678.6:c.2959A>C
|
ENSP00000412835.2:p.Arg987=
|
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NM_017519.2:c.4393A>C
|
NP_059989.2:p.Arg1465=
|
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NM_020732.3:c.4432A>C
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NP_065783.3:p.Arg1478=
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XM_005267069.3:c.4552A>C
|
XP_005267126.2:p.Arg1518=
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XM_011535984.1:c.3631A>C
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XP_011534286.1:p.Arg1211=
|
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XM_011535985.1:c.3451A>C
|
XP_011534287.1:p.Arg1151=
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XM_011535986.1:c.3211A>C
|
XP_011534288.1:p.Arg1071=
|
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XM_011535987.1:c.2830A>C
|
XP_011534289.1:p.Arg944=
|
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XM_011535988.1:c.1693A>C
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XP_011534290.1:p.Arg565=
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NM_001346813.1:c.4552A>C
|
NP_001333742.1:p.Arg1518=
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NM_001363725.1:c.2302A>C
|
NP_001350654.1:p.Arg768=
|
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XM_011535984.2:c.4762A>C
|
XP_011534286.2:p.Arg1588=
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XM_011535988.3:c.1693A>C
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XP_011534290.1:p.Arg565=
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XM_017011103.2:c.4663A>C
|
XP_016866592.1:p.Arg1555=
|
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XM_017011104.1:c.4633A>C
|
XP_016866593.1:p.Arg1545=
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XM_017011105.2:c.4603A>C
|
XP_016866594.1:p.Arg1535=
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XM_017011106.2:c.4474A>C
|
XP_016866595.1:p.Arg1492=
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XM_017011107.2:c.4453A>C
|
XP_016866596.1:p.Arg1485=
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XR_002956289.1:n.4748A>C
|
|
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NM_001363725.2:c.2302A>C
|
NP_001350654.1:p.Arg768=
|
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NM_001371656.1:c.4681A>C
|
NP_001358585.1:p.Arg1561=
|
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NM_001374820.1:c.4681A>C
|
NP_001361749.1:p.Arg1561=
|
|
NM_001374828.1:c.4801A>C
MANE Select
|
NP_001361757.1:p.Arg1601=
|
|
NM_017519.3:c.4642A>C
|
NP_059989.3:p.Arg1548=
|
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