ENST00000350026.11:c.4566G>T
|
ENSP00000055163.8:p.Leu1522=
|
|
ENST00000414678.8:c.4635G>T
|
ENSP00000412835.3:p.Leu1545=
|
|
ENST00000637015.2:c.4854G>T
|
ENSP00000489729.2:p.Leu1618=
|
|
ENST00000346085.10:c.4605G>T
|
ENSP00000344546.5:p.Leu1535=
|
|
ENST00000350026.10:c.4317G>T
|
ENSP00000055163.7:p.Leu1439=
|
|
ENST00000414678.7:c.2883G>T
|
ENSP00000412835.2:p.Leu961=
|
|
ENST00000635849.1:c.2046G>T
|
ENSP00000490948.1:p.Leu682=
|
|
ENST00000635957.1:c.1677G>T
|
ENSP00000490385.1:p.Leu559=
|
|
ENST00000636227.1:n.3188G>T
|
|
|
ENST00000636254.1:n.645G>T
|
|
|
ENST00000636930.2:c.4725G>T
MANE Select
|
ENSP00000490491.2:p.Leu1575=
|
|
ENST00000636940.1:n.2722G>T
|
|
|
ENST00000637015.1:c.2093G>T
|
|
|
ENST00000637568.1:c.2007G>T
|
|
|
ENST00000637741.1:n.1391G>T
|
|
|
ENST00000637810.1:c.2067G>T
|
ENSP00000489636.1:p.Leu689=
|
|
ENST00000637904.1:c.2226G>T
|
ENSP00000490550.1:p.Leu742=
|
|
ENST00000647938.1:c.4356G>T
|
ENSP00000498155.1:p.Leu1452=
|
|
ENST00000346085.9:c.4356G>T
|
ENSP00000344546.4:p.Leu1452=
|
|
ENST00000350026.9:c.4317G>T
|
ENSP00000055163.7:p.Leu1439=
|
|
ENST00000414678.6:c.2883G>T
|
ENSP00000412835.2:p.Leu961=
|
|
NM_017519.2:c.4317G>T
|
NP_059989.2:p.Leu1439=
|
|
NM_020732.3:c.4356G>T
|
NP_065783.3:p.Leu1452=
|
|
XM_005267069.3:c.4476G>T
|
XP_005267126.2:p.Leu1492=
|
|
XM_011535984.1:c.3555G>T
|
XP_011534286.1:p.Leu1185=
|
|
XM_011535985.1:c.3375G>T
|
XP_011534287.1:p.Leu1125=
|
|
XM_011535986.1:c.3135G>T
|
XP_011534288.1:p.Leu1045=
|
|
XM_011535987.1:c.2754G>T
|
XP_011534289.1:p.Leu918=
|
|
XM_011535988.1:c.1617G>T
|
XP_011534290.1:p.Leu539=
|
|
NM_001346813.1:c.4476G>T
|
NP_001333742.1:p.Leu1492=
|
|
NM_001363725.1:c.2226G>T
|
NP_001350654.1:p.Leu742=
|
|
XM_011535984.2:c.4686G>T
|
XP_011534286.2:p.Leu1562=
|
|
XM_011535988.3:c.1617G>T
|
XP_011534290.1:p.Leu539=
|
|
XM_017011103.2:c.4587G>T
|
XP_016866592.1:p.Leu1529=
|
|
XM_017011104.1:c.4557G>T
|
XP_016866593.1:p.Leu1519=
|
|
XM_017011105.2:c.4527G>T
|
XP_016866594.1:p.Leu1509=
|
|
XM_017011106.2:c.4398G>T
|
XP_016866595.1:p.Leu1466=
|
|
XM_017011107.2:c.4377G>T
|
XP_016866596.1:p.Leu1459=
|
|
XR_002956289.1:n.4672G>T
|
|
|
NM_001363725.2:c.2226G>T
|
NP_001350654.1:p.Leu742=
|
|
NM_001371656.1:c.4605G>T
|
NP_001358585.1:p.Leu1535=
|
|
NM_001374820.1:c.4605G>T
|
NP_001361749.1:p.Leu1535=
|
|
NM_001374828.1:c.4725G>T
MANE Select
|
NP_001361757.1:p.Leu1575=
|
|
NM_017519.3:c.4566G>T
|
NP_059989.3:p.Leu1522=
|
|