ENST00000350026.11:c.3963G>T
|
ENSP00000055163.8:p.Arg1321=
|
|
ENST00000414678.8:c.4032G>T
|
ENSP00000412835.3:p.Arg1344=
|
|
ENST00000637015.2:c.4251G>T
|
ENSP00000489729.2:p.Arg1417=
|
|
ENST00000346085.10:c.4002G>T
|
ENSP00000344546.5:p.Arg1334=
|
|
ENST00000350026.10:c.3714G>T
|
ENSP00000055163.7:p.Arg1238=
|
|
ENST00000414678.7:c.2280G>T
|
ENSP00000412835.2:p.Arg760=
|
|
ENST00000635849.1:c.1443G>T
|
ENSP00000490948.1:p.Arg481=
|
|
ENST00000635957.1:c.1074G>T
|
ENSP00000490385.1:p.Arg358=
|
|
ENST00000636930.2:c.4122G>T
MANE Select
|
ENSP00000490491.2:p.Arg1374=
|
|
ENST00000636940.1:n.2119G>T
|
|
|
ENST00000637015.1:c.1490G>T
|
|
|
ENST00000637568.1:c.1404G>T
|
|
|
ENST00000637741.1:n.788G>T
|
|
|
ENST00000637810.1:c.1464G>T
|
ENSP00000489636.1:p.Arg488=
|
|
ENST00000637904.1:c.1623G>T
|
ENSP00000490550.1:p.Arg541=
|
|
ENST00000647938.1:c.3753G>T
|
ENSP00000498155.1:p.Arg1251=
|
|
ENST00000346085.9:c.3753G>T
|
ENSP00000344546.4:p.Arg1251=
|
|
ENST00000350026.9:c.3714G>T
|
ENSP00000055163.7:p.Arg1238=
|
|
ENST00000414678.6:c.2280G>T
|
ENSP00000412835.2:p.Arg760=
|
|
NM_017519.2:c.3714G>T
|
NP_059989.2:p.Arg1238=
|
|
NM_020732.3:c.3753G>T
|
NP_065783.3:p.Arg1251=
|
|
XM_005267069.3:c.3873G>T
|
XP_005267126.2:p.Arg1291=
|
|
XM_011535984.1:c.2952G>T
|
XP_011534286.1:p.Arg984=
|
|
XM_011535985.1:c.2772G>T
|
XP_011534287.1:p.Arg924=
|
|
XM_011535986.1:c.2532G>T
|
XP_011534288.1:p.Arg844=
|
|
XM_011535987.1:c.2151G>T
|
XP_011534289.1:p.Arg717=
|
|
XM_011535988.1:c.1014G>T
|
XP_011534290.1:p.Arg338=
|
|
NM_001346813.1:c.3873G>T
|
NP_001333742.1:p.Arg1291=
|
|
NM_001363725.1:c.1623G>T
|
NP_001350654.1:p.Arg541=
|
|
XM_011535984.2:c.4083G>T
|
XP_011534286.2:p.Arg1361=
|
|
XM_011535988.3:c.1014G>T
|
XP_011534290.1:p.Arg338=
|
|
XM_017011103.2:c.3984G>T
|
XP_016866592.1:p.Arg1328=
|
|
XM_017011104.1:c.3954G>T
|
XP_016866593.1:p.Arg1318=
|
|
XM_017011105.2:c.3924G>T
|
XP_016866594.1:p.Arg1308=
|
|
XM_017011106.2:c.3795G>T
|
XP_016866595.1:p.Arg1265=
|
|
XM_017011107.2:c.3774G>T
|
XP_016866596.1:p.Arg1258=
|
|
XR_002956289.1:n.4166G>T
|
|
|
NM_001363725.2:c.1623G>T
|
NP_001350654.1:p.Arg541=
|
|
NM_001371656.1:c.4002G>T
|
NP_001358585.1:p.Arg1334=
|
|
NM_001374820.1:c.4002G>T
|
NP_001361749.1:p.Arg1334=
|
|
NM_001374828.1:c.4122G>T
MANE Select
|
NP_001361757.1:p.Arg1374=
|
|
NM_017519.3:c.3963G>T
|
NP_059989.3:p.Arg1321=
|
|