ENST00000348974.5:c.879T>C
|
ENSP00000330021.7:p.Leu293=
|
|
ENST00000394236.9:c.879T>C
MANE Select
|
ENSP00000377783.3:p.Leu293=
|
|
ENST00000407433.6:c.834T>C
|
ENSP00000385794.2:p.Leu278=
|
|
ENST00000647936.1:c.879T>C
|
ENSP00000496822.1:p.Leu293=
|
|
ENST00000648381.1:n.1047T>C
|
|
|
ENST00000648853.1:c.837T>C
|
ENSP00000497262.1:p.Leu279=
|
|
ENST00000649103.1:c.978T>C
|
ENSP00000497962.1:n.978T>C
|
|
ENST00000650591.1:c.975T>C
|
ENSP00000497376.1:p.Leu325=
|
|
ENST00000394236.7:c.879T>C
|
ENSP00000377783.3:p.Leu293=
|
|
ENST00000407433.5:c.486T>C
|
ENSP00000385794.1:p.Leu162=
|
|
NM_000313.3:c.879T>C , LRG_572t1:c.879T>C
|
NP_000304.2:p.Leu293=
|
|
NM_001314077.1:c.975T>C , LRG_572t2:c.975T>C
|
NP_001301006.1:p.Leu325=
|
|
NM_000313.4:c.879T>C
MANE Select
|
NP_000304.2:p.Leu293=
|
|
NM_001314077.2:c.975T>C
|
NP_001301006.1:p.Leu325=
|
|