ENST00000526817.2:c.496+5G>A
|
ENSP00000432145.2:n.496+5G>A
|
|
ENST00000314134.4:c.535+5G>A
MANE Select
|
ENSP00000313318.3:n.535+5G>A
|
|
ENST00000314134.3:c.535+5G>A
|
ENSP00000313318.3:n.535+5G>A
|
|
ENST00000442528.2:c.496+5G>A
|
ENSP00000412408.2:n.496+5G>A
|
|
NM_001145265.1:c.496+5G>A
|
NP_001138737.1:n.496+5G>A
|
|
NM_001145266.1:c.496+5G>A
|
NP_001138738.1:n.496+5G>A
|
|
NM_018389.4:c.535+5G>A , LRG_107t1:c.535+5G>A
|
NP_060859.4:n.535+5G>A
|
|
XM_011520203.1:c.535+5G>A
|
XP_011518505.1:n.535+5G>A
|
|
XM_011520203.3:c.535+5G>A
|
XP_011518505.1:n.535+5G>A
|
|
NM_001145265.2:c.496+5G>A
|
NP_001138737.1:n.496+5G>A
|
|
NM_018389.5:c.535+5G>A
MANE Select
|
NP_060859.4:n.535+5G>A
|
|