|
ENST00000350026.11:c.5614C>T
|
ENSP00000055163.8:p.Arg1872Ter
|
|
|
ENST00000414678.8:c.5683C>T
|
ENSP00000412835.3:p.Arg1895Ter
|
|
|
ENST00000637015.2:c.5902C>T
|
ENSP00000489729.2:p.Arg1968Ter
|
|
|
ENST00000346085.10:c.5653C>T
|
ENSP00000344546.5:p.Arg1885Ter
|
|
|
ENST00000350026.10:c.5365C>T
|
ENSP00000055163.7:p.Arg1789Ter
|
|
|
ENST00000414678.7:c.3931C>T
|
ENSP00000412835.2:p.Arg1311Ter
|
|
|
ENST00000635849.1:c.3094C>T
|
ENSP00000490948.1:p.Arg1032Ter
|
|
|
ENST00000635957.1:c.2725C>T
|
ENSP00000490385.1:p.Arg909Ter
|
|
|
ENST00000636227.1:n.4236C>T
|
|
|
|
ENST00000636254.1:n.1693C>T
|
|
|
|
ENST00000636930.2:c.5773C>T
MANE Select
|
ENSP00000490491.2:p.Arg1925Ter
|
|
|
ENST00000636940.1:n.3770C>T
|
|
|
|
ENST00000637015.1:c.3141C>T
|
|
|
|
ENST00000637568.1:c.3055C>T
|
|
|
|
ENST00000637741.1:n.2439C>T
|
|
|
|
ENST00000637810.1:c.3115C>T
|
ENSP00000489636.1:p.Arg1039Ter
|
|
|
ENST00000637904.1:c.3274C>T
|
ENSP00000490550.1:p.Arg1092Ter
|
|
|
ENST00000637933.1:n.2888C>T
|
|
|
|
ENST00000647938.1:c.5404C>T
|
ENSP00000498155.1:p.Arg1802Ter
|
|
|
ENST00000346085.9:c.5404C>T
|
ENSP00000344546.4:p.Arg1802Ter
|
|
|
ENST00000350026.9:c.5365C>T
|
ENSP00000055163.7:p.Arg1789Ter
|
|
|
ENST00000414678.6:c.3931C>T
|
ENSP00000412835.2:p.Arg1311Ter
|
|
|
NM_017519.2:c.5365C>T
|
NP_059989.2:p.Arg1789Ter
|
|
|
NM_020732.3:c.5404C>T
|
NP_065783.3:p.Arg1802Ter
|
|
|
XM_005267069.3:c.5524C>T
|
XP_005267126.2:p.Arg1842Ter
|
|
|
XM_011535984.1:c.4603C>T
|
XP_011534286.1:p.Arg1535Ter
|
|
|
XM_011535985.1:c.4423C>T
|
XP_011534287.1:p.Arg1475Ter
|
|
|
XM_011535986.1:c.4183C>T
|
XP_011534288.1:p.Arg1395Ter
|
|
|
XM_011535987.1:c.3802C>T
|
XP_011534289.1:p.Arg1268Ter
|
|
|
XM_011535988.1:c.2665C>T
|
XP_011534290.1:p.Arg889Ter
|
|
|
NM_001346813.1:c.5524C>T
|
NP_001333742.1:p.Arg1842Ter
|
|
|
NM_001363725.1:c.3274C>T
|
NP_001350654.1:p.Arg1092Ter
|
|
|
XM_011535984.2:c.5734C>T
|
XP_011534286.2:p.Arg1912Ter
|
|
|
XM_011535988.3:c.2665C>T
|
XP_011534290.1:p.Arg889Ter
|
|
|
XM_017011103.2:c.5635C>T
|
XP_016866592.1:p.Arg1879Ter
|
|
|
XM_017011104.1:c.5605C>T
|
XP_016866593.1:p.Arg1869Ter
|
|
|
XM_017011105.2:c.5575C>T
|
XP_016866594.1:p.Arg1859Ter
|
|
|
XM_017011106.2:c.5446C>T
|
XP_016866595.1:p.Arg1816Ter
|
|
|
XM_017011107.2:c.5425C>T
|
XP_016866596.1:p.Arg1809Ter
|
|
|
XR_002956289.1:n.5720C>T
|
|
|
|
NM_001363725.2:c.3274C>T
|
NP_001350654.1:p.Arg1092Ter
|
|
|
NM_001371656.1:c.5653C>T
|
NP_001358585.1:p.Arg1885Ter
|
|
|
NM_001374820.1:c.5653C>T
|
NP_001361749.1:p.Arg1885Ter
|
|
|
NM_001374828.1:c.5773C>T
MANE Select
|
NP_001361757.1:p.Arg1925Ter
|
|
|
NM_017519.3:c.5614C>T
|
NP_059989.3:p.Arg1872Ter
|
|
