ENST00000470094.2:c.*445T>C
|
ENSP00000434898.2:n.*445T>C
|
|
ENST00000528762.2:c.*1289T>C
|
ENSP00000433168.2:n.*1289T>C
|
|
ENST00000530893.7:c.9553T>C
|
ENSP00000499438.2:p.Tyr3185His
|
|
ENST00000665585.2:c.*1484T>C
|
ENSP00000499570.2:n.*1484T>C
|
|
ENST00000700202.2:c.9871T>C
|
ENSP00000514856.2:p.Tyr3291His
|
|
ENST00000700202.1:c.2338T>C
|
ENSP00000514856.1:p.Tyr780His
|
|
ENST00000700203.1:n.2049T>C
|
|
|
ENST00000380152.8:c.9922T>C
MANE Select
|
ENSP00000369497.3:p.Tyr3308His
|
|
ENST00000544455.6:c.9922T>C
|
ENSP00000439902.1:p.Tyr3308His
|
|
ENST00000614259.2:c.9930T>C
|
ENSP00000506251.1:n.9930T>C
|
|
ENST00000680887.1:c.9922T>C
|
ENSP00000505508.1:p.Tyr3308His
|
|
ENST00000380152.7:c.9922T>C
|
ENSP00000369497.3:p.Tyr3308His
|
|
ENST00000533776.1:n.510T>C
|
|
|
ENST00000544455.5:c.9922T>C
|
ENSP00000439902.1:p.Tyr3308His
|
|
NM_000059.3:c.9922T>C , LRG_293t1:c.9922T>C
|
NP_000050.2:p.Tyr3308His
|
|
XM_011535203.1:c.9922T>C
|
XP_011533505.1:p.Tyr3308His
|
|
XM_011535204.1:c.9826T>C
|
XP_011533506.1:p.Tyr3276His
|
|
NM_000059.4:c.9922T>C
MANE Select
|
NP_000050.3:p.Tyr3308His
|
|