ENST00000350026.11:c.4503G>C
|
ENSP00000055163.8:p.Arg1501Ser
|
|
ENST00000414678.8:c.4572G>C
|
ENSP00000412835.3:p.Arg1524Ser
|
|
ENST00000637015.2:c.4791G>C
|
ENSP00000489729.2:p.Arg1597Ser
|
|
ENST00000346085.10:c.4542G>C
|
ENSP00000344546.5:p.Arg1514Ser
|
|
ENST00000350026.10:c.4254G>C
|
ENSP00000055163.7:p.Arg1418Ser
|
|
ENST00000414678.7:c.2820G>C
|
ENSP00000412835.2:p.Arg940Ser
|
|
ENST00000635849.1:c.1983G>C
|
ENSP00000490948.1:p.Arg661Ser
|
|
ENST00000635957.1:c.1614G>C
|
ENSP00000490385.1:p.Arg538Ser
|
|
ENST00000636227.1:n.3125G>C
|
|
|
ENST00000636254.1:n.582G>C
|
|
|
ENST00000636930.2:c.4662G>C
MANE Select
|
ENSP00000490491.2:p.Arg1554Ser
|
|
ENST00000636940.1:n.2659G>C
|
|
|
ENST00000637015.1:c.2030G>C
|
|
|
ENST00000637568.1:c.1944G>C
|
|
|
ENST00000637741.1:n.1328G>C
|
|
|
ENST00000637810.1:c.2004G>C
|
ENSP00000489636.1:p.Arg668Ser
|
|
ENST00000637904.1:c.2163G>C
|
ENSP00000490550.1:p.Arg721Ser
|
|
ENST00000647938.1:c.4293G>C
|
ENSP00000498155.1:p.Arg1431Ser
|
|
ENST00000346085.9:c.4293G>C
|
ENSP00000344546.4:p.Arg1431Ser
|
|
ENST00000350026.9:c.4254G>C
|
ENSP00000055163.7:p.Arg1418Ser
|
|
ENST00000414678.6:c.2820G>C
|
ENSP00000412835.2:p.Arg940Ser
|
|
NM_017519.2:c.4254G>C
|
NP_059989.2:p.Arg1418Ser
|
|
NM_020732.3:c.4293G>C
|
NP_065783.3:p.Arg1431Ser
|
|
XM_005267069.3:c.4413G>C
|
XP_005267126.2:p.Arg1471Ser
|
|
XM_011535984.1:c.3492G>C
|
XP_011534286.1:p.Arg1164Ser
|
|
XM_011535985.1:c.3312G>C
|
XP_011534287.1:p.Arg1104Ser
|
|
XM_011535986.1:c.3072G>C
|
XP_011534288.1:p.Arg1024Ser
|
|
XM_011535987.1:c.2691G>C
|
XP_011534289.1:p.Arg897Ser
|
|
XM_011535988.1:c.1554G>C
|
XP_011534290.1:p.Arg518Ser
|
|
NM_001346813.1:c.4413G>C
|
NP_001333742.1:p.Arg1471Ser
|
|
NM_001363725.1:c.2163G>C
|
NP_001350654.1:p.Arg721Ser
|
|
XM_011535984.2:c.4623G>C
|
XP_011534286.2:p.Arg1541Ser
|
|
XM_011535988.3:c.1554G>C
|
XP_011534290.1:p.Arg518Ser
|
|
XM_017011103.2:c.4524G>C
|
XP_016866592.1:p.Arg1508Ser
|
|
XM_017011104.1:c.4494G>C
|
XP_016866593.1:p.Arg1498Ser
|
|
XM_017011105.2:c.4464G>C
|
XP_016866594.1:p.Arg1488Ser
|
|
XM_017011106.2:c.4335G>C
|
XP_016866595.1:p.Arg1445Ser
|
|
XM_017011107.2:c.4314G>C
|
XP_016866596.1:p.Arg1438Ser
|
|
XR_002956289.1:n.4609G>C
|
|
|
NM_001363725.2:c.2163G>C
|
NP_001350654.1:p.Arg721Ser
|
|
NM_001371656.1:c.4542G>C
|
NP_001358585.1:p.Arg1514Ser
|
|
NM_001374820.1:c.4542G>C
|
NP_001361749.1:p.Arg1514Ser
|
|
NM_001374828.1:c.4662G>C
MANE Select
|
NP_001361757.1:p.Arg1554Ser
|
|
NM_017519.3:c.4503G>C
|
NP_059989.3:p.Arg1501Ser
|
|