ENST00000350026.11:c.3508C>G
|
ENSP00000055163.8:p.Leu1170Val
|
|
ENST00000414678.8:c.3577C>G
|
ENSP00000412835.3:p.Leu1193Val
|
|
ENST00000637015.2:c.3796C>G
|
ENSP00000489729.2:p.Leu1266Val
|
|
ENST00000319584.11:c.1681C>G
|
ENSP00000313006.7:p.Leu561Val
|
|
ENST00000346085.10:c.3547C>G
|
ENSP00000344546.5:p.Leu1183Val
|
|
ENST00000350026.10:c.3259C>G
|
ENSP00000055163.7:p.Leu1087Val
|
|
ENST00000414678.7:c.1825C>G
|
ENSP00000412835.2:p.Leu609Val
|
|
ENST00000635849.1:c.988C>G
|
ENSP00000490948.1:p.Leu330Val
|
|
ENST00000635957.1:c.622C>G
|
ENSP00000490385.1:p.Leu208Val
|
|
ENST00000636930.2:c.3667C>G
MANE Select
|
ENSP00000490491.2:p.Leu1223Val
|
|
ENST00000636940.1:n.1664C>G
|
|
|
ENST00000637015.1:c.1035C>G
|
|
|
ENST00000637568.1:c.949C>G
|
|
|
ENST00000637741.1:n.333C>G
|
|
|
ENST00000637810.1:c.1009C>G
|
ENSP00000489636.1:p.Leu337Val
|
|
ENST00000637904.1:c.1168C>G
|
ENSP00000490550.1:p.Leu390Val
|
|
ENST00000647938.1:c.3298C>G
|
ENSP00000498155.1:p.Leu1100Val
|
|
ENST00000319584.10:c.1684C>G
|
ENSP00000313006.6:p.Leu562Val
|
|
ENST00000346085.9:c.3298C>G
|
ENSP00000344546.4:p.Leu1100Val
|
|
ENST00000350026.9:c.3259C>G
|
ENSP00000055163.7:p.Leu1087Val
|
|
ENST00000400790.3:c.460C>G
|
ENSP00000383596.3:p.Leu154Val
|
|
ENST00000414678.6:c.1825C>G
|
ENSP00000412835.2:p.Leu609Val
|
|
ENST00000478761.3:c.869C>G
|
|
|
NM_017519.2:c.3259C>G
|
NP_059989.2:p.Leu1087Val
|
|
NM_020732.3:c.3298C>G
|
NP_065783.3:p.Leu1100Val
|
|
XM_005267069.3:c.3418C>G
|
XP_005267126.2:p.Leu1140Val
|
|
XM_011535984.1:c.2497C>G
|
XP_011534286.1:p.Leu833Val
|
|
XM_011535985.1:c.2317C>G
|
XP_011534287.1:p.Leu773Val
|
|
XM_011535986.1:c.2077C>G
|
XP_011534288.1:p.Leu693Val
|
|
XM_011535987.1:c.1696C>G
|
XP_011534289.1:p.Leu566Val
|
|
XM_011535988.1:c.559C>G
|
XP_011534290.1:p.Leu187Val
|
|
NM_001346813.1:c.3418C>G
|
NP_001333742.1:p.Leu1140Val
|
|
NM_001363725.1:c.1168C>G
|
NP_001350654.1:p.Leu390Val
|
|
XM_011535984.2:c.3628C>G
|
XP_011534286.2:p.Leu1210Val
|
|
XM_011535988.3:c.559C>G
|
XP_011534290.1:p.Leu187Val
|
|
XM_017011103.2:c.3529C>G
|
XP_016866592.1:p.Leu1177Val
|
|
XM_017011104.1:c.3499C>G
|
XP_016866593.1:p.Leu1167Val
|
|
XM_017011105.2:c.3469C>G
|
XP_016866594.1:p.Leu1157Val
|
|
XM_017011106.2:c.3340C>G
|
XP_016866595.1:p.Leu1114Val
|
|
XM_017011107.2:c.3319C>G
|
XP_016866596.1:p.Leu1107Val
|
|
XR_002956289.1:n.3711C>G
|
|
|
NM_001363725.2:c.1168C>G
|
NP_001350654.1:p.Leu390Val
|
|
NM_001371656.1:c.3547C>G
|
NP_001358585.1:p.Leu1183Val
|
|
NM_001374820.1:c.3547C>G
|
NP_001361749.1:p.Leu1183Val
|
|
NM_001374828.1:c.3667C>G
MANE Select
|
NP_001361757.1:p.Leu1223Val
|
|
NM_017519.3:c.3508C>G
|
NP_059989.3:p.Leu1170Val
|
|