ENST00000691183.1:c.*409-1G>A
|
ENSP00000509954.1:n.*409-1G>A
|
|
ENST00000378842.8:c.821-1G>A
MANE Select
|
ENSP00000368119.4:n.821-1G>A
|
|
ENST00000378842.7:c.821-1G>A
|
ENSP00000368119.3:n.821-1G>A
|
|
ENST00000450095.6:c.494-1G>A
|
ENSP00000401956.2:n.494-1G>A
|
|
ENST00000488412.2:n.76G>A
|
|
|
ENST00000489643.6:n.901-1G>A
|
|
|
ENST00000554085.5:c.*565-1G>A
|
ENSP00000450419.1:n.*565-1G>A
|
|
ENST00000554550.5:c.*441-1G>A
|
ENSP00000451435.1:n.*441-1G>A
|
|
ENST00000554638.5:n.1293-1G>A
|
|
|
ENST00000555020.5:n.1282-1G>A
|
|
|
ENST00000555086.5:n.927G>A
|
|
|
ENST00000555754.1:n.268G>A
|
|
|
ENST00000556278.1:c.432+541G>A
|
ENSP00000451792.1:n.432+541G>A
|
|
ENST00000557706.5:n.1396-1G>A
|
|
|
NM_000155.3:c.821-1G>A
|
NP_000146.2:n.821-1G>A
|
|
NM_001258332.1:c.494-1G>A
|
NP_001245261.1:n.494-1G>A
|
|
NM_000155.4:c.821-1G>A
MANE Select
|
NP_000146.2:n.821-1G>A
|
|
NM_001258332.2:c.494-1G>A
|
NP_001245261.1:n.494-1G>A
|
|