ENST00000477226.6:n.646T=
|
|
|
ENST00000683013.1:n.560T=
|
|
|
ENST00000373960.4:c.1172T=
MANE Select
|
ENSP00000363071.3:p.Leu391=
|
|
ENST00000373960.3:c.1172T=
|
ENSP00000363071.3:p.Leu391=
|
|
ENST00000477226.5:n.644T=
|
|
|
ENST00000492726.1:n.567T=
|
|
|
NM_001927.3:c.1172T= , LRG_380t1:c.1172T=
|
NP_001918.3:p.Leu391=
|
|
NM_001927.4:c.1172T=
MANE Select
|
NP_001918.3:p.Leu391=
|
|
NM_001382708.1:c.1169T=
|
NP_001369637.1:p.Leu390=
|
|
NM_001382709.1:c.740T=
|
NP_001369638.1:p.Leu247=
|
|
NM_001382710.1:c.1103T=
|
NP_001369639.1:p.Leu368=
|
|
NM_001382711.1:c.1151T=
|
NP_001369640.1:p.Leu384=
|
|
NM_001382712.1:c.1172T=
|
NP_001369641.1:p.Leu391=
|
|
NM_001382713.1:c.902T=
|
NP_001369642.1:p.Leu301=
|
|