|
NM_020863.4:c.2887+2350G=
MANE Select
|
NP_065914.2:n.2887+2350G=
|
|
ENST00000377838.8:c.2887+2350G=
MANE Select
|
ENSP00000367069.3:n.2887+2350G=
|
|
NM_001029939.3:c.2851+2350G=
|
NP_001025110.2:n.2851+2350G=
|
|
NM_001029939.4:c.2851+2350G=
|
NP_001025110.2:n.2851+2350G=
|
|
NM_001167583.2:c.2851+2350G=
|
NP_001161055.1:n.2851+2350G=
|
|
NM_001167583.3:c.2851+2350G=
|
NP_001161055.1:n.2851+2350G=
|
|
NM_001174157.1:c.2701+2350G=
|
NP_001167628.1:n.2701+2350G=
|
|
NM_001174157.2:c.2701+2350G=
|
NP_001167628.1:n.2701+2350G=
|
|
NM_001174158.1:c.2851+2350G=
|
NP_001167629.1:n.2851+2350G=
|
|
NM_001174158.2:c.2851+2350G=
|
NP_001167629.1:n.2851+2350G=
|
|
NM_001289394.1:c.2851+2350G=
|
NP_001276323.1:n.2851+2350G=
|
|
NM_001289394.2:c.2851+2350G=
|
NP_001276323.1:n.2851+2350G=
|
|
NM_020863.3:c.2887+2350G=
|
NP_065914.2:n.2887+2350G=
|
|
NR_110323.1:n.3073+2350G=
|
|
|
NR_110323.2:n.3055+2350G=
|
|
|
ENST00000377838.7:c.2887+2350G=
|
ENSP00000367069.3:n.2887+2350G=
|
|
ENST00000429442.6:c.2851+2350G=
|
ENSP00000394501.2:n.2851+2350G=
|
|
ENST00000517307.5:n.491+2350G=
|
|
|
ENST00000520214.5:c.2851+2350G=
|
ENSP00000428483.1:n.2851+2350G=
|
|
ENST00000520356.5:c.2851+2350G=
|
ENSP00000427879.1:n.2851+2350G=
|
|
ENST00000520727.5:c.2851+2350G=
|
ENSP00000427831.1:n.2851+2350G=
|
|
ENST00000523243.5:c.2887+2350G=
|
ENSP00000429930.1:n.2887+2350G=
|
|
ENST00000523399.5:c.2701+2350G=
|
ENSP00000429091.1:n.2701+2350G=
|
|
ENST00000523924.5:c.*2869+2350G=
|
ENSP00000429050.1:n.*2869+2350G=
|
|
XM_011517203.1:c.2851+2350G=
|
XP_011515505.1:n.2851+2350G=
|
|
XM_011517204.1:c.2701+2350G=
|
XP_011515506.1:n.2701+2350G=
|
|
XM_011517204.2:c.2701+2350G=
|
XP_011515506.1:n.2701+2350G=
|
|
XM_011517206.1:c.2851+2350G=
|
XP_011515508.1:n.2851+2350G=
|
|
XM_011517206.2:c.2851+2350G=
|
XP_011515508.1:n.2851+2350G=
|
|
XM_017013716.1:c.2851+2350G=
|
XP_016869205.1:n.2851+2350G=
|
|
XR_001745568.1:n.2868+2350G=
|
|
|
XR_001745569.1:n.2868+2350G=
|
|
|
XR_928343.1:n.2868+2350G=
|
|
|
XR_928343.2:n.2868+2350G=
|
|
