ENST00000470094.2:c.*225G>A
|
ENSP00000434898.2:n.*225G>A
|
|
ENST00000528762.2:c.*1069G>A
|
ENSP00000433168.2:n.*1069G>A
|
|
ENST00000530893.7:c.9333G>A
|
ENSP00000499438.2:p.Met3111Ile
|
|
ENST00000665585.2:c.*1264G>A
|
ENSP00000499570.2:n.*1264G>A
|
|
ENST00000700202.2:c.9651G>A
|
ENSP00000514856.2:p.Met3217Ile
|
|
ENST00000700202.1:c.2118G>A
|
ENSP00000514856.1:p.Met706Ile
|
|
ENST00000700203.1:n.1829G>A
|
|
|
ENST00000380152.8:c.9702G>A
MANE Select
|
ENSP00000369497.3:p.Met3234Ile
|
|
ENST00000544455.6:c.9702G>A
|
ENSP00000439902.1:p.Met3234Ile
|
|
ENST00000614259.2:c.9710G>A
|
ENSP00000506251.1:n.9710G>A
|
|
ENST00000665585.1:c.2580G>A
|
|
|
ENST00000680887.1:c.9702G>A
|
ENSP00000505508.1:p.Met3234Ile
|
|
ENST00000380152.7:c.9702G>A
|
ENSP00000369497.3:p.Met3234Ile
|
|
ENST00000470094.1:c.785G>A
|
|
|
ENST00000533776.1:n.290G>A
|
|
|
ENST00000544455.5:c.9702G>A
|
ENSP00000439902.1:p.Met3234Ile
|
|
NM_000059.3:c.9702G>A , LRG_293t1:c.9702G>A
|
NP_000050.2:p.Met3234Ile
|
|
XM_011535203.1:c.9702G>A
|
XP_011533505.1:p.Met3234Ile
|
|
XM_011535204.1:c.9606G>A
|
XP_011533506.1:p.Met3202Ile
|
|
NM_000059.4:c.9702G>A
MANE Select
|
NP_000050.3:p.Met3234Ile
|
|