ENST00000348974.5:c.1821G=
|
ENSP00000330021.7:p.Leu607=
|
|
ENST00000394236.9:c.1821G=
MANE Select
|
ENSP00000377783.3:p.Leu607=
|
|
ENST00000407433.6:c.1776G=
|
ENSP00000385794.2:p.Leu592=
|
|
ENST00000647936.1:c.1644+2148G=
|
ENSP00000496822.1:n.1644+2148G=
|
|
ENST00000648381.1:n.1989G=
|
|
|
ENST00000648853.1:c.1779G=
|
ENSP00000497262.1:p.Leu593=
|
|
ENST00000649585.1:c.764G=
|
ENSP00000498163.1:n.764G=
|
|
ENST00000650591.1:c.1917G=
|
ENSP00000497376.1:p.Leu639=
|
|
ENST00000394236.7:c.1821G=
|
ENSP00000377783.3:p.Leu607=
|
|
ENST00000407433.5:c.1428G=
|
ENSP00000385794.1:p.Leu476=
|
|
NM_000313.3:c.1821G= , LRG_572t1:c.1821G=
|
NP_000304.2:p.Leu607=
|
|
NM_001314077.1:c.1917G= , LRG_572t2:c.1917G=
|
NP_001301006.1:p.Leu639=
|
|
NM_000313.4:c.1821G=
MANE Select
|
NP_000304.2:p.Leu607=
|
|
NM_001314077.2:c.1917G=
|
NP_001301006.1:p.Leu639=
|
|