|
ENST00000350026.11:c.4546C>T
|
ENSP00000055163.8:p.Gln1516Ter
|
|
|
ENST00000414678.8:c.4615C>T
|
ENSP00000412835.3:p.Gln1539Ter
|
|
|
ENST00000637015.2:c.4834C>T
|
ENSP00000489729.2:p.Gln1612Ter
|
|
|
ENST00000346085.10:c.4585C>T
|
ENSP00000344546.5:p.Gln1529Ter
|
|
|
ENST00000350026.10:c.4297C>T
|
ENSP00000055163.7:p.Gln1433Ter
|
|
|
ENST00000414678.7:c.2863C>T
|
ENSP00000412835.2:p.Gln955Ter
|
|
|
ENST00000635849.1:c.2026C>T
|
ENSP00000490948.1:p.Gln676Ter
|
|
|
ENST00000635957.1:c.1657C>T
|
ENSP00000490385.1:p.Gln553Ter
|
|
|
ENST00000636227.1:n.3168C>T
|
|
|
|
ENST00000636254.1:n.625C>T
|
|
|
|
ENST00000636930.2:c.4705C>T
MANE Select
|
ENSP00000490491.2:p.Gln1569Ter
|
|
|
ENST00000636940.1:n.2702C>T
|
|
|
|
ENST00000637015.1:c.2073C>T
|
|
|
|
ENST00000637568.1:c.1987C>T
|
|
|
|
ENST00000637741.1:n.1371C>T
|
|
|
|
ENST00000637810.1:c.2047C>T
|
ENSP00000489636.1:p.Gln683Ter
|
|
|
ENST00000637904.1:c.2206C>T
|
ENSP00000490550.1:p.Gln736Ter
|
|
|
ENST00000647938.1:c.4336C>T
|
ENSP00000498155.1:p.Gln1446Ter
|
|
|
ENST00000346085.9:c.4336C>T
|
ENSP00000344546.4:p.Gln1446Ter
|
|
|
ENST00000350026.9:c.4297C>T
|
ENSP00000055163.7:p.Gln1433Ter
|
|
|
ENST00000414678.6:c.2863C>T
|
ENSP00000412835.2:p.Gln955Ter
|
|
|
NM_017519.2:c.4297C>T
|
NP_059989.2:p.Gln1433Ter
|
|
|
NM_020732.3:c.4336C>T
|
NP_065783.3:p.Gln1446Ter
|
|
|
XM_005267069.3:c.4456C>T
|
XP_005267126.2:p.Gln1486Ter
|
|
|
XM_011535984.1:c.3535C>T
|
XP_011534286.1:p.Gln1179Ter
|
|
|
XM_011535985.1:c.3355C>T
|
XP_011534287.1:p.Gln1119Ter
|
|
|
XM_011535986.1:c.3115C>T
|
XP_011534288.1:p.Gln1039Ter
|
|
|
XM_011535987.1:c.2734C>T
|
XP_011534289.1:p.Gln912Ter
|
|
|
XM_011535988.1:c.1597C>T
|
XP_011534290.1:p.Gln533Ter
|
|
|
NM_001346813.1:c.4456C>T
|
NP_001333742.1:p.Gln1486Ter
|
|
|
NM_001363725.1:c.2206C>T
|
NP_001350654.1:p.Gln736Ter
|
|
|
XM_011535984.2:c.4666C>T
|
XP_011534286.2:p.Gln1556Ter
|
|
|
XM_011535988.3:c.1597C>T
|
XP_011534290.1:p.Gln533Ter
|
|
|
XM_017011103.2:c.4567C>T
|
XP_016866592.1:p.Gln1523Ter
|
|
|
XM_017011104.1:c.4537C>T
|
XP_016866593.1:p.Gln1513Ter
|
|
|
XM_017011105.2:c.4507C>T
|
XP_016866594.1:p.Gln1503Ter
|
|
|
XM_017011106.2:c.4378C>T
|
XP_016866595.1:p.Gln1460Ter
|
|
|
XM_017011107.2:c.4357C>T
|
XP_016866596.1:p.Gln1453Ter
|
|
|
XR_002956289.1:n.4652C>T
|
|
|
|
NM_001363725.2:c.2206C>T
|
NP_001350654.1:p.Gln736Ter
|
|
|
NM_001371656.1:c.4585C>T
|
NP_001358585.1:p.Gln1529Ter
|
|
|
NM_001374820.1:c.4585C>T
|
NP_001361749.1:p.Gln1529Ter
|
|
|
NM_001374828.1:c.4705C>T
MANE Select
|
NP_001361757.1:p.Gln1569Ter
|
|
|
NM_017519.3:c.4546C>T
|
NP_059989.3:p.Gln1516Ter
|
|
