|
NM_005630.3:c.1106-1G>A
MANE Select
|
NP_005621.2:n.1106-1G>A
|
|
ENST00000310926.11:c.1106-1G>A
MANE Select
|
ENSP00000311291.4:n.1106-1G>A
|
|
NM_005630.2:c.1106-1G>A
|
NP_005621.2:n.1106-1G>A
|
|
ENST00000310926.8:c.1106-1G>A
|
ENSP00000311291.4:n.1106-1G>A
|
|
ENST00000462770.5:n.686-1G>A
|
|
|
ENST00000481359.3:c.1105+1090G>A
|
ENSP00000420028.3:n.1105+1090G>A
|
|
ENST00000493729.5:c.878-1G>A
|
ENSP00000418893.1:n.878-1G>A
|
|
XM_011513090.1:c.1106-1G>A
|
XP_011511392.1:n.1106-1G>A
|
|
XM_017007077.1:c.602-1G>A
|
XP_016862566.1:n.602-1G>A
|
|
XM_024453721.1:c.1106-1G>A
|
XP_024309489.1:n.1106-1G>A
|