ENST00000470094.2:c.9265C>A
|
ENSP00000434898.2:p.Pro3089Thr
|
|
ENST00000528762.2:c.*632C>A
|
ENSP00000433168.2:n.*632C>A
|
|
ENST00000530893.7:c.8896C>A
|
ENSP00000499438.2:p.Pro2966Thr
|
|
ENST00000665585.2:c.*827C>A
|
ENSP00000499570.2:n.*827C>A
|
|
ENST00000666593.2:c.*110C>A
|
ENSP00000499256.2:n.*110C>A
|
|
ENST00000700202.2:c.9214C>A
|
ENSP00000514856.2:p.Pro3072Thr
|
|
ENST00000700202.1:c.1681C>A
|
ENSP00000514856.1:p.Pro561Thr
|
|
ENST00000700203.1:n.1392C>A
|
|
|
ENST00000380152.8:c.9265C>A
MANE Select
|
ENSP00000369497.3:p.Pro3089Thr
|
|
ENST00000544455.6:c.9265C>A
|
ENSP00000439902.1:p.Pro3089Thr
|
|
ENST00000614259.2:c.9273C>A
|
ENSP00000506251.1:n.9273C>A
|
|
ENST00000665585.1:c.2143C>A
|
|
|
ENST00000666593.1:c.287C>A
|
ENSP00000499256.1:n.287C>A
|
|
ENST00000680887.1:c.9265C>A
|
ENSP00000505508.1:p.Pro3089Thr
|
|
ENST00000380152.7:c.9265C>A
|
ENSP00000369497.3:p.Pro3089Thr
|
|
ENST00000470094.1:c.222C>A
|
|
|
ENST00000544455.5:c.9265C>A
|
ENSP00000439902.1:p.Pro3089Thr
|
|
NM_000059.3:c.9265C>A , LRG_293t1:c.9265C>A
|
NP_000050.2:p.Pro3089Thr
|
|
XM_011535203.1:c.9265C>A
|
XP_011533505.1:p.Pro3089Thr
|
|
XM_011535204.1:c.9169C>A
|
XP_011533506.1:p.Pro3057Thr
|
|
NM_000059.4:c.9265C>A
MANE Select
|
NP_000050.3:p.Pro3089Thr
|
|