|
NM_000154.2:c.1107+1G>A
MANE Select
|
NP_000145.1:n.1107+1G>A
|
|
ENST00000588479.6:c.1107+1G>A
MANE Select
|
ENSP00000465930.1:n.1107+1G>A
|
|
NM_000154.1:c.1107+1G>A
|
NP_000145.1:n.1107+1G>A
|
|
NM_001381985.1:c.1107+1G>A
|
NP_001368914.1:n.1107+1G>A
|
|
ENST00000225614.6:c.1107+1G>A
|
ENSP00000225614.1:n.1107+1G>A
|
|
ENST00000586733.1:n.309+1G>A
|
|
|
ENST00000588479.5:c.1107+1G>A
|
ENSP00000465930.1:n.1107+1G>A
|
|
ENST00000589643.1:n.161-82G>A
|
|
|
ENST00000592997.5:c.483+1G>A
|
ENSP00000464765.1:n.483+1G>A
|
|
ENST00000592997.6:c.1017+1G>A
|
ENSP00000464765.2:n.1017+1G>A
|