ENST00000350026.11:c.3398T>G
|
ENSP00000055163.8:p.Leu1133Arg
|
|
ENST00000414678.8:c.3467T>G
|
ENSP00000412835.3:p.Leu1156Arg
|
|
ENST00000637015.2:c.3686T>G
|
ENSP00000489729.2:p.Leu1229Arg
|
|
ENST00000319584.11:c.1571T>G
|
ENSP00000313006.7:p.Leu524Arg
|
|
ENST00000346085.10:c.3437T>G
|
ENSP00000344546.5:p.Leu1146Arg
|
|
ENST00000350026.10:c.3149T>G
|
ENSP00000055163.7:p.Leu1050Arg
|
|
ENST00000414678.7:c.1715T>G
|
ENSP00000412835.2:p.Leu572Arg
|
|
ENST00000635849.1:c.878T>G
|
ENSP00000490948.1:p.Leu293Arg
|
|
ENST00000635957.1:c.512T>G
|
ENSP00000490385.1:p.Leu171Arg
|
|
ENST00000636930.2:c.3557T>G
MANE Select
|
ENSP00000490491.2:p.Leu1186Arg
|
|
ENST00000636940.1:n.1554T>G
|
|
|
ENST00000637015.1:c.925T>G
|
|
|
ENST00000637568.1:c.839T>G
|
|
|
ENST00000637741.1:n.223T>G
|
|
|
ENST00000637810.1:c.899T>G
|
ENSP00000489636.1:p.Leu300Arg
|
|
ENST00000637904.1:c.1058T>G
|
ENSP00000490550.1:p.Leu353Arg
|
|
ENST00000647938.1:c.3188T>G
|
ENSP00000498155.1:p.Leu1063Arg
|
|
ENST00000319584.10:c.1574T>G
|
ENSP00000313006.6:p.Leu525Arg
|
|
ENST00000346085.9:c.3188T>G
|
ENSP00000344546.4:p.Leu1063Arg
|
|
ENST00000350026.9:c.3149T>G
|
ENSP00000055163.7:p.Leu1050Arg
|
|
ENST00000400790.3:c.350T>G
|
ENSP00000383596.3:p.Leu117Arg
|
|
ENST00000414678.6:c.1715T>G
|
ENSP00000412835.2:p.Leu572Arg
|
|
ENST00000478761.3:c.759T>G
|
|
|
NM_017519.2:c.3149T>G
|
NP_059989.2:p.Leu1050Arg
|
|
NM_020732.3:c.3188T>G
|
NP_065783.3:p.Leu1063Arg
|
|
XM_005267069.3:c.3308T>G
|
XP_005267126.2:p.Leu1103Arg
|
|
XM_011535984.1:c.2387T>G
|
XP_011534286.1:p.Leu796Arg
|
|
XM_011535985.1:c.2207T>G
|
XP_011534287.1:p.Leu736Arg
|
|
XM_011535986.1:c.1967T>G
|
XP_011534288.1:p.Leu656Arg
|
|
XM_011535987.1:c.1586T>G
|
XP_011534289.1:p.Leu529Arg
|
|
XM_011535988.1:c.449T>G
|
XP_011534290.1:p.Leu150Arg
|
|
NM_001346813.1:c.3308T>G
|
NP_001333742.1:p.Leu1103Arg
|
|
NM_001363725.1:c.1058T>G
|
NP_001350654.1:p.Leu353Arg
|
|
XM_011535984.2:c.3518T>G
|
XP_011534286.2:p.Leu1173Arg
|
|
XM_011535988.3:c.449T>G
|
XP_011534290.1:p.Leu150Arg
|
|
XM_017011103.2:c.3419T>G
|
XP_016866592.1:p.Leu1140Arg
|
|
XM_017011104.1:c.3389T>G
|
XP_016866593.1:p.Leu1130Arg
|
|
XM_017011105.2:c.3359T>G
|
XP_016866594.1:p.Leu1120Arg
|
|
XM_017011106.2:c.3230T>G
|
XP_016866595.1:p.Leu1077Arg
|
|
XM_017011107.2:c.3209T>G
|
XP_016866596.1:p.Leu1070Arg
|
|
XR_002956289.1:n.3601T>G
|
|
|
NM_001363725.2:c.1058T>G
|
NP_001350654.1:p.Leu353Arg
|
|
NM_001371656.1:c.3437T>G
|
NP_001358585.1:p.Leu1146Arg
|
|
NM_001374820.1:c.3437T>G
|
NP_001361749.1:p.Leu1146Arg
|
|
NM_001374828.1:c.3557T>G
MANE Select
|
NP_001361757.1:p.Leu1186Arg
|
|
NM_017519.3:c.3398T>G
|
NP_059989.3:p.Leu1133Arg
|
|