ENST00000470094.2:c.*75G>T
|
ENSP00000434898.2:n.*75G>T
|
|
ENST00000528762.2:c.*919G>T
|
ENSP00000433168.2:n.*919G>T
|
|
ENST00000530893.7:c.9183G>T
|
ENSP00000499438.2:p.Leu3061=
|
|
ENST00000665585.2:c.*1114G>T
|
ENSP00000499570.2:n.*1114G>T
|
|
ENST00000700202.2:c.9501G>T
|
ENSP00000514856.2:p.Leu3167=
|
|
ENST00000700202.1:c.1968G>T
|
ENSP00000514856.1:p.Leu656=
|
|
ENST00000700203.1:n.1679G>T
|
|
|
ENST00000380152.8:c.9552G>T
MANE Select
|
ENSP00000369497.3:p.Leu3184=
|
|
ENST00000544455.6:c.9552G>T
|
ENSP00000439902.1:p.Leu3184=
|
|
ENST00000614259.2:c.9560G>T
|
ENSP00000506251.1:n.9560G>T
|
|
ENST00000665585.1:c.2430G>T
|
|
|
ENST00000680887.1:c.9552G>T
|
ENSP00000505508.1:p.Leu3184=
|
|
ENST00000380152.7:c.9552G>T
|
ENSP00000369497.3:p.Leu3184=
|
|
ENST00000470094.1:c.635G>T
|
|
|
ENST00000533776.1:n.140G>T
|
|
|
ENST00000544455.5:c.9552G>T
|
ENSP00000439902.1:p.Leu3184=
|
|
NM_000059.3:c.9552G>T , LRG_293t1:c.9552G>T
|
NP_000050.2:p.Leu3184=
|
|
XM_011535203.1:c.9552G>T
|
XP_011533505.1:p.Leu3184=
|
|
XM_011535204.1:c.9456G>T
|
XP_011533506.1:p.Leu3152=
|
|
NM_000059.4:c.9552G>T
MANE Select
|
NP_000050.3:p.Leu3184=
|
|