ENST00000348974.5:c.880G>T
|
ENSP00000330021.7:p.Asp294Tyr
|
|
ENST00000394236.9:c.880G>T
MANE Select
|
ENSP00000377783.3:p.Asp294Tyr
|
|
ENST00000407433.6:c.835G>T
|
ENSP00000385794.2:p.Asp279Tyr
|
|
ENST00000647936.1:c.880G>T
|
ENSP00000496822.1:p.Asp294Tyr
|
|
ENST00000648381.1:n.1048G>T
|
|
|
ENST00000648853.1:c.838G>T
|
ENSP00000497262.1:p.Asp280Tyr
|
|
ENST00000649103.1:c.979G>T
|
ENSP00000497962.1:n.979G>T
|
|
ENST00000650591.1:c.976G>T
|
ENSP00000497376.1:p.Asp326Tyr
|
|
ENST00000394236.7:c.880G>T
|
ENSP00000377783.3:p.Asp294Tyr
|
|
ENST00000407433.5:c.487G>T
|
ENSP00000385794.1:p.Asp163Tyr
|
|
NM_000313.3:c.880G>T , LRG_572t1:c.880G>T
|
NP_000304.2:p.Asp294Tyr
|
|
NM_001314077.1:c.976G>T , LRG_572t2:c.976G>T
|
NP_001301006.1:p.Asp326Tyr
|
|
NM_000313.4:c.880G>T
MANE Select
|
NP_000304.2:p.Asp294Tyr
|
|
NM_001314077.2:c.976G>T
|
NP_001301006.1:p.Asp326Tyr
|
|