ENST00000310926.11:c.397+10T>C
MANE Select
|
ENSP00000311291.4:n.397+10T>C
|
|
ENST00000310926.8:c.397+10T>C
|
ENSP00000311291.4:n.397+10T>C
|
|
ENST00000462770.5:n.520+10T>C
|
|
|
ENST00000464676.5:n.659+10T>C
|
|
|
ENST00000478651.1:n.520+10T>C
|
|
|
ENST00000481359.3:c.397+10T>C
|
ENSP00000420028.3:n.397+10T>C
|
|
ENST00000493729.5:c.397+10T>C
|
ENSP00000418893.1:n.397+10T>C
|
|
NM_005630.2:c.397+10T>C
|
NP_005621.2:n.397+10T>C
|
|
XM_011513090.1:c.397+10T>C
|
XP_011511392.1:n.397+10T>C
|
|
XM_017007077.1:c.-108+10T>C
|
XP_016862566.1:n.-108+10T>C
|
|
XM_024453721.1:c.397+10T>C
|
XP_024309489.1:n.397+10T>C
|
|
NM_005630.3:c.397+10T>C
MANE Select
|
NP_005621.2:n.397+10T>C
|
|