ENST00000470094.2:c.*305A>T
|
ENSP00000434898.2:n.*305A>T
|
|
ENST00000528762.2:c.*1149A>T
|
ENSP00000433168.2:n.*1149A>T
|
|
ENST00000530893.7:c.9413A>T
|
ENSP00000499438.2:p.Asp3138Val
|
|
ENST00000665585.2:c.*1344A>T
|
ENSP00000499570.2:n.*1344A>T
|
|
ENST00000700202.2:c.9731A>T
|
ENSP00000514856.2:p.Asp3244Val
|
|
ENST00000700202.1:c.2198A>T
|
ENSP00000514856.1:p.Asp733Val
|
|
ENST00000700203.1:n.1909A>T
|
|
|
ENST00000380152.8:c.9782A>T
MANE Select
|
ENSP00000369497.3:p.Asp3261Val
|
|
ENST00000544455.6:c.9782A>T
|
ENSP00000439902.1:p.Asp3261Val
|
|
ENST00000614259.2:c.9790A>T
|
ENSP00000506251.1:n.9790A>T
|
|
ENST00000680887.1:c.9782A>T
|
ENSP00000505508.1:p.Asp3261Val
|
|
ENST00000380152.7:c.9782A>T
|
ENSP00000369497.3:p.Asp3261Val
|
|
ENST00000533776.1:n.370A>T
|
|
|
ENST00000544455.5:c.9782A>T
|
ENSP00000439902.1:p.Asp3261Val
|
|
NM_000059.3:c.9782A>T , LRG_293t1:c.9782A>T
|
NP_000050.2:p.Asp3261Val
|
|
XM_011535203.1:c.9782A>T
|
XP_011533505.1:p.Asp3261Val
|
|
XM_011535204.1:c.9686A>T
|
XP_011533506.1:p.Asp3229Val
|
|
NM_000059.4:c.9782A>T
MANE Select
|
NP_000050.3:p.Asp3261Val
|
|