ENST00000350026.11:c.3961C>T
|
ENSP00000055163.8:p.Arg1321Trp
|
|
ENST00000414678.8:c.4030C>T
|
ENSP00000412835.3:p.Arg1344Trp
|
|
ENST00000637015.2:c.4249C>T
|
ENSP00000489729.2:p.Arg1417Trp
|
|
ENST00000346085.10:c.4000C>T
|
ENSP00000344546.5:p.Arg1334Trp
|
|
ENST00000350026.10:c.3712C>T
|
ENSP00000055163.7:p.Arg1238Trp
|
|
ENST00000414678.7:c.2278C>T
|
ENSP00000412835.2:p.Arg760Trp
|
|
ENST00000635849.1:c.1441C>T
|
ENSP00000490948.1:p.Arg481Trp
|
|
ENST00000635957.1:c.1072C>T
|
ENSP00000490385.1:p.Arg358Trp
|
|
ENST00000636930.2:c.4120C>T
MANE Select
|
ENSP00000490491.2:p.Arg1374Trp
|
|
ENST00000636940.1:n.2117C>T
|
|
|
ENST00000637015.1:c.1488C>T
|
|
|
ENST00000637568.1:c.1402C>T
|
|
|
ENST00000637741.1:n.786C>T
|
|
|
ENST00000637810.1:c.1462C>T
|
ENSP00000489636.1:p.Arg488Trp
|
|
ENST00000637904.1:c.1621C>T
|
ENSP00000490550.1:p.Arg541Trp
|
|
ENST00000647938.1:c.3751C>T
|
ENSP00000498155.1:p.Arg1251Trp
|
|
ENST00000346085.9:c.3751C>T
|
ENSP00000344546.4:p.Arg1251Trp
|
|
ENST00000350026.9:c.3712C>T
|
ENSP00000055163.7:p.Arg1238Trp
|
|
ENST00000414678.6:c.2278C>T
|
ENSP00000412835.2:p.Arg760Trp
|
|
NM_017519.2:c.3712C>T
|
NP_059989.2:p.Arg1238Trp
|
|
NM_020732.3:c.3751C>T
|
NP_065783.3:p.Arg1251Trp
|
|
XM_005267069.3:c.3871C>T
|
XP_005267126.2:p.Arg1291Trp
|
|
XM_011535984.1:c.2950C>T
|
XP_011534286.1:p.Arg984Trp
|
|
XM_011535985.1:c.2770C>T
|
XP_011534287.1:p.Arg924Trp
|
|
XM_011535986.1:c.2530C>T
|
XP_011534288.1:p.Arg844Trp
|
|
XM_011535987.1:c.2149C>T
|
XP_011534289.1:p.Arg717Trp
|
|
XM_011535988.1:c.1012C>T
|
XP_011534290.1:p.Arg338Trp
|
|
NM_001346813.1:c.3871C>T
|
NP_001333742.1:p.Arg1291Trp
|
|
NM_001363725.1:c.1621C>T
|
NP_001350654.1:p.Arg541Trp
|
|
XM_011535984.2:c.4081C>T
|
XP_011534286.2:p.Arg1361Trp
|
|
XM_011535988.3:c.1012C>T
|
XP_011534290.1:p.Arg338Trp
|
|
XM_017011103.2:c.3982C>T
|
XP_016866592.1:p.Arg1328Trp
|
|
XM_017011104.1:c.3952C>T
|
XP_016866593.1:p.Arg1318Trp
|
|
XM_017011105.2:c.3922C>T
|
XP_016866594.1:p.Arg1308Trp
|
|
XM_017011106.2:c.3793C>T
|
XP_016866595.1:p.Arg1265Trp
|
|
XM_017011107.2:c.3772C>T
|
XP_016866596.1:p.Arg1258Trp
|
|
XR_002956289.1:n.4164C>T
|
|
|
NM_001363725.2:c.1621C>T
|
NP_001350654.1:p.Arg541Trp
|
|
NM_001371656.1:c.4000C>T
|
NP_001358585.1:p.Arg1334Trp
|
|
NM_001374820.1:c.4000C>T
|
NP_001361749.1:p.Arg1334Trp
|
|
NM_001374828.1:c.4120C>T
MANE Select
|
NP_001361757.1:p.Arg1374Trp
|
|
NM_017519.3:c.3961C>T
|
NP_059989.3:p.Arg1321Trp
|
|