ENST00000350026.11:c.4741C>T
|
ENSP00000055163.8:p.Gln1581Ter
|
|
ENST00000414678.8:c.4810C>T
|
ENSP00000412835.3:p.Gln1604Ter
|
|
ENST00000637015.2:c.5029C>T
|
ENSP00000489729.2:p.Gln1677Ter
|
|
ENST00000346085.10:c.4780C>T
|
ENSP00000344546.5:p.Gln1594Ter
|
|
ENST00000350026.10:c.4492C>T
|
ENSP00000055163.7:p.Gln1498Ter
|
|
ENST00000414678.7:c.3058C>T
|
ENSP00000412835.2:p.Gln1020Ter
|
|
ENST00000635849.1:c.2221C>T
|
ENSP00000490948.1:p.Gln741Ter
|
|
ENST00000635957.1:c.1852C>T
|
ENSP00000490385.1:p.Gln618Ter
|
|
ENST00000636227.1:n.3363C>T
|
|
|
ENST00000636254.1:n.820C>T
|
|
|
ENST00000636930.2:c.4900C>T
MANE Select
|
ENSP00000490491.2:p.Gln1634Ter
|
|
ENST00000636940.1:n.2897C>T
|
|
|
ENST00000637015.1:c.2268C>T
|
|
|
ENST00000637568.1:c.2182C>T
|
|
|
ENST00000637741.1:n.1566C>T
|
|
|
ENST00000637810.1:c.2242C>T
|
ENSP00000489636.1:p.Gln748Ter
|
|
ENST00000637904.1:c.2401C>T
|
ENSP00000490550.1:p.Gln801Ter
|
|
ENST00000647938.1:c.4531C>T
|
ENSP00000498155.1:p.Gln1511Ter
|
|
ENST00000346085.9:c.4531C>T
|
ENSP00000344546.4:p.Gln1511Ter
|
|
ENST00000350026.9:c.4492C>T
|
ENSP00000055163.7:p.Gln1498Ter
|
|
ENST00000414678.6:c.3058C>T
|
ENSP00000412835.2:p.Gln1020Ter
|
|
NM_017519.2:c.4492C>T
|
NP_059989.2:p.Gln1498Ter
|
|
NM_020732.3:c.4531C>T
|
NP_065783.3:p.Gln1511Ter
|
|
XM_005267069.3:c.4651C>T
|
XP_005267126.2:p.Gln1551Ter
|
|
XM_011535984.1:c.3730C>T
|
XP_011534286.1:p.Gln1244Ter
|
|
XM_011535985.1:c.3550C>T
|
XP_011534287.1:p.Gln1184Ter
|
|
XM_011535986.1:c.3310C>T
|
XP_011534288.1:p.Gln1104Ter
|
|
XM_011535987.1:c.2929C>T
|
XP_011534289.1:p.Gln977Ter
|
|
XM_011535988.1:c.1792C>T
|
XP_011534290.1:p.Gln598Ter
|
|
NM_001346813.1:c.4651C>T
|
NP_001333742.1:p.Gln1551Ter
|
|
NM_001363725.1:c.2401C>T
|
NP_001350654.1:p.Gln801Ter
|
|
XM_011535984.2:c.4861C>T
|
XP_011534286.2:p.Gln1621Ter
|
|
XM_011535988.3:c.1792C>T
|
XP_011534290.1:p.Gln598Ter
|
|
XM_017011103.2:c.4762C>T
|
XP_016866592.1:p.Gln1588Ter
|
|
XM_017011104.1:c.4732C>T
|
XP_016866593.1:p.Gln1578Ter
|
|
XM_017011105.2:c.4702C>T
|
XP_016866594.1:p.Gln1568Ter
|
|
XM_017011106.2:c.4573C>T
|
XP_016866595.1:p.Gln1525Ter
|
|
XM_017011107.2:c.4552C>T
|
XP_016866596.1:p.Gln1518Ter
|
|
XR_002956289.1:n.4847C>T
|
|
|
NM_001363725.2:c.2401C>T
|
NP_001350654.1:p.Gln801Ter
|
|
NM_001371656.1:c.4780C>T
|
NP_001358585.1:p.Gln1594Ter
|
|
NM_001374820.1:c.4780C>T
|
NP_001361749.1:p.Gln1594Ter
|
|
NM_001374828.1:c.4900C>T
MANE Select
|
NP_001361757.1:p.Gln1634Ter
|
|
NM_017519.3:c.4741C>T
|
NP_059989.3:p.Gln1581Ter
|
|