|
ENST00000615310.5:c.1390C>A
|
ENSP00000480088.2:p.Pro464Thr
|
|
|
ENST00000683007.1:n.1360C>A
|
|
|
|
ENST00000683872.1:n.547C>A
|
|
|
|
ENST00000340058.6:c.1786C>A
|
ENSP00000344798.4:p.Pro596Thr
|
|
|
ENST00000355710.8:c.1786C>A
MANE Select
|
ENSP00000347942.3:p.Pro596Thr
|
|
|
ENST00000671844.1:c.*380C>A
|
ENSP00000500541.1:n.*380C>A
|
|
|
ENST00000672389.1:c.*380C>A
|
ENSP00000500252.1:n.*380C>A
|
|
|
ENST00000340058.5:c.1786C>A
|
ENSP00000344798.4:p.Pro596Thr
|
|
|
ENST00000355710.7:c.1786C>A
|
ENSP00000347942.3:p.Pro596Thr
|
|
|
ENST00000498820.5:c.337C>A
|
ENSP00000419080.1:p.Pro113Thr
|
|
|
ENST00000615310.4:c.1289+2350C>A
|
ENSP00000480088.1:n.1289+2350C>A
|
|
|
NM_020630.4:c.1786C>A , LRG_518t2:c.1786C>A
|
NP_065681.1:p.Pro596Thr
|
|
|
NM_020975.4:c.1786C>A , LRG_518t1:c.1786C>A
|
NP_066124.1:p.Pro596Thr
|
|
|
XM_011540027.1:c.1786C>A
|
XP_011538329.1:p.Pro596Thr
|
|
|
NM_001355216.1:c.1024C>A
|
NP_001342145.1:p.Pro342Thr
|
|
|
NM_020630.5:c.1786C>A
|
NP_065681.1:p.Pro596Thr
|
|
|
NM_020975.5:c.1786C>A
|
NP_066124.1:p.Pro596Thr
|
|
|
NM_020975.6:c.1786C>A
MANE Select
|
NP_066124.1:p.Pro596Thr
|
|
|
NM_020630.6:c.1786C>A
|
NP_065681.1:p.Pro596Thr
|
|
