ENST00000350026.11:c.4893C>T
|
ENSP00000055163.8:p.Arg1631=
|
|
ENST00000414678.8:c.4962C>T
|
ENSP00000412835.3:p.Arg1654=
|
|
ENST00000637015.2:c.5181C>T
|
ENSP00000489729.2:p.Arg1727=
|
|
ENST00000346085.10:c.4932C>T
|
ENSP00000344546.5:p.Arg1644=
|
|
ENST00000350026.10:c.4644C>T
|
ENSP00000055163.7:p.Arg1548=
|
|
ENST00000414678.7:c.3210C>T
|
ENSP00000412835.2:p.Arg1070=
|
|
ENST00000635849.1:c.2373C>T
|
ENSP00000490948.1:p.Arg791=
|
|
ENST00000635957.1:c.2004C>T
|
ENSP00000490385.1:p.Arg668=
|
|
ENST00000636227.1:n.3515C>T
|
|
|
ENST00000636254.1:n.972C>T
|
|
|
ENST00000636930.2:c.5052C>T
MANE Select
|
ENSP00000490491.2:p.Arg1684=
|
|
ENST00000636940.1:n.3049C>T
|
|
|
ENST00000637015.1:c.2420C>T
|
|
|
ENST00000637568.1:c.2334C>T
|
|
|
ENST00000637741.1:n.1718C>T
|
|
|
ENST00000637810.1:c.2394C>T
|
ENSP00000489636.1:p.Arg798=
|
|
ENST00000637904.1:c.2553C>T
|
ENSP00000490550.1:p.Arg851=
|
|
ENST00000647938.1:c.4683C>T
|
ENSP00000498155.1:p.Arg1561=
|
|
ENST00000346085.9:c.4683C>T
|
ENSP00000344546.4:p.Arg1561=
|
|
ENST00000350026.9:c.4644C>T
|
ENSP00000055163.7:p.Arg1548=
|
|
ENST00000414678.6:c.3210C>T
|
ENSP00000412835.2:p.Arg1070=
|
|
NM_017519.2:c.4644C>T
|
NP_059989.2:p.Arg1548=
|
|
NM_020732.3:c.4683C>T
|
NP_065783.3:p.Arg1561=
|
|
XM_005267069.3:c.4803C>T
|
XP_005267126.2:p.Arg1601=
|
|
XM_011535984.1:c.3882C>T
|
XP_011534286.1:p.Arg1294=
|
|
XM_011535985.1:c.3702C>T
|
XP_011534287.1:p.Arg1234=
|
|
XM_011535986.1:c.3462C>T
|
XP_011534288.1:p.Arg1154=
|
|
XM_011535987.1:c.3081C>T
|
XP_011534289.1:p.Arg1027=
|
|
XM_011535988.1:c.1944C>T
|
XP_011534290.1:p.Arg648=
|
|
NM_001346813.1:c.4803C>T
|
NP_001333742.1:p.Arg1601=
|
|
NM_001363725.1:c.2553C>T
|
NP_001350654.1:p.Arg851=
|
|
XM_011535984.2:c.5013C>T
|
XP_011534286.2:p.Arg1671=
|
|
XM_011535988.3:c.1944C>T
|
XP_011534290.1:p.Arg648=
|
|
XM_017011103.2:c.4914C>T
|
XP_016866592.1:p.Arg1638=
|
|
XM_017011104.1:c.4884C>T
|
XP_016866593.1:p.Arg1628=
|
|
XM_017011105.2:c.4854C>T
|
XP_016866594.1:p.Arg1618=
|
|
XM_017011106.2:c.4725C>T
|
XP_016866595.1:p.Arg1575=
|
|
XM_017011107.2:c.4704C>T
|
XP_016866596.1:p.Arg1568=
|
|
XR_002956289.1:n.4999C>T
|
|
|
NM_001363725.2:c.2553C>T
|
NP_001350654.1:p.Arg851=
|
|
NM_001371656.1:c.4932C>T
|
NP_001358585.1:p.Arg1644=
|
|
NM_001374820.1:c.4932C>T
|
NP_001361749.1:p.Arg1644=
|
|
NM_001374828.1:c.5052C>T
MANE Select
|
NP_001361757.1:p.Arg1684=
|
|
NM_017519.3:c.4893C>T
|
NP_059989.3:p.Arg1631=
|
|