ENST00000691183.1:c.*492+5G>A
|
ENSP00000509954.1:n.*492+5G>A
|
|
ENST00000378842.8:c.904+5G>A
MANE Select
|
ENSP00000368119.4:n.904+5G>A
|
|
ENST00000378842.7:c.904+5G>A
|
ENSP00000368119.3:n.904+5G>A
|
|
ENST00000450095.6:c.577+5G>A
|
ENSP00000401956.2:n.577+5G>A
|
|
ENST00000488412.2:n.165G>A
|
|
|
ENST00000489643.6:n.989G>A
|
|
|
ENST00000554550.5:c.*524+5G>A
|
ENSP00000451435.1:n.*524+5G>A
|
|
ENST00000554638.5:n.1376+5G>A
|
|
|
ENST00000555020.5:n.1370G>A
|
|
|
ENST00000555086.5:n.1016G>A
|
|
|
ENST00000555754.1:n.352+5G>A
|
|
|
ENST00000556278.1:c.432+630G>A
|
ENSP00000451792.1:n.432+630G>A
|
|
ENST00000557706.5:n.1479+5G>A
|
|
|
NM_000155.3:c.904+5G>A
|
NP_000146.2:n.904+5G>A
|
|
NM_001258332.1:c.577+5G>A
|
NP_001245261.1:n.577+5G>A
|
|
NM_000155.4:c.904+5G>A
MANE Select
|
NP_000146.2:n.904+5G>A
|
|
NM_001258332.2:c.577+5G>A
|
NP_001245261.1:n.577+5G>A
|
|