ENST00000350026.11:c.3548T>G
|
ENSP00000055163.8:p.Leu1183Trp
|
|
ENST00000414678.8:c.3617T>G
|
ENSP00000412835.3:p.Leu1206Trp
|
|
ENST00000637015.2:c.3836T>G
|
ENSP00000489729.2:p.Leu1279Trp
|
|
ENST00000319584.11:c.1721T>G
|
ENSP00000313006.7:p.Leu574Trp
|
|
ENST00000346085.10:c.3587T>G
|
ENSP00000344546.5:p.Leu1196Trp
|
|
ENST00000350026.10:c.3299T>G
|
ENSP00000055163.7:p.Leu1100Trp
|
|
ENST00000414678.7:c.1865T>G
|
ENSP00000412835.2:p.Leu622Trp
|
|
ENST00000635849.1:c.1028T>G
|
ENSP00000490948.1:p.Leu343Trp
|
|
ENST00000635957.1:c.662T>G
|
ENSP00000490385.1:p.Leu221Trp
|
|
ENST00000636930.2:c.3707T>G
MANE Select
|
ENSP00000490491.2:p.Leu1236Trp
|
|
ENST00000636940.1:n.1704T>G
|
|
|
ENST00000637015.1:c.1075T>G
|
|
|
ENST00000637568.1:c.989T>G
|
|
|
ENST00000637741.1:n.373T>G
|
|
|
ENST00000637810.1:c.1049T>G
|
ENSP00000489636.1:p.Leu350Trp
|
|
ENST00000637904.1:c.1208T>G
|
ENSP00000490550.1:p.Leu403Trp
|
|
ENST00000647938.1:c.3338T>G
|
ENSP00000498155.1:p.Leu1113Trp
|
|
ENST00000319584.10:c.1724T>G
|
ENSP00000313006.6:p.Leu575Trp
|
|
ENST00000346085.9:c.3338T>G
|
ENSP00000344546.4:p.Leu1113Trp
|
|
ENST00000350026.9:c.3299T>G
|
ENSP00000055163.7:p.Leu1100Trp
|
|
ENST00000400790.3:c.500T>G
|
ENSP00000383596.3:p.Leu167Trp
|
|
ENST00000414678.6:c.1865T>G
|
ENSP00000412835.2:p.Leu622Trp
|
|
ENST00000478761.3:c.909T>G
|
|
|
NM_017519.2:c.3299T>G
|
NP_059989.2:p.Leu1100Trp
|
|
NM_020732.3:c.3338T>G
|
NP_065783.3:p.Leu1113Trp
|
|
XM_005267069.3:c.3458T>G
|
XP_005267126.2:p.Leu1153Trp
|
|
XM_011535984.1:c.2537T>G
|
XP_011534286.1:p.Leu846Trp
|
|
XM_011535985.1:c.2357T>G
|
XP_011534287.1:p.Leu786Trp
|
|
XM_011535986.1:c.2117T>G
|
XP_011534288.1:p.Leu706Trp
|
|
XM_011535987.1:c.1736T>G
|
XP_011534289.1:p.Leu579Trp
|
|
XM_011535988.1:c.599T>G
|
XP_011534290.1:p.Leu200Trp
|
|
NM_001346813.1:c.3458T>G
|
NP_001333742.1:p.Leu1153Trp
|
|
NM_001363725.1:c.1208T>G
|
NP_001350654.1:p.Leu403Trp
|
|
XM_011535984.2:c.3668T>G
|
XP_011534286.2:p.Leu1223Trp
|
|
XM_011535988.3:c.599T>G
|
XP_011534290.1:p.Leu200Trp
|
|
XM_017011103.2:c.3569T>G
|
XP_016866592.1:p.Leu1190Trp
|
|
XM_017011104.1:c.3539T>G
|
XP_016866593.1:p.Leu1180Trp
|
|
XM_017011105.2:c.3509T>G
|
XP_016866594.1:p.Leu1170Trp
|
|
XM_017011106.2:c.3380T>G
|
XP_016866595.1:p.Leu1127Trp
|
|
XM_017011107.2:c.3359T>G
|
XP_016866596.1:p.Leu1120Trp
|
|
XR_002956289.1:n.3751T>G
|
|
|
NM_001363725.2:c.1208T>G
|
NP_001350654.1:p.Leu403Trp
|
|
NM_001371656.1:c.3587T>G
|
NP_001358585.1:p.Leu1196Trp
|
|
NM_001374820.1:c.3587T>G
|
NP_001361749.1:p.Leu1196Trp
|
|
NM_001374828.1:c.3707T>G
MANE Select
|
NP_001361757.1:p.Leu1236Trp
|
|
NM_017519.3:c.3548T>G
|
NP_059989.3:p.Leu1183Trp
|
|