ENST00000470094.2:c.*85G>C
|
ENSP00000434898.2:n.*85G>C
|
|
ENST00000528762.2:c.*929G>C
|
ENSP00000433168.2:n.*929G>C
|
|
ENST00000530893.7:c.9193G>C
|
ENSP00000499438.2:p.Asp3065His
|
|
ENST00000665585.2:c.*1124G>C
|
ENSP00000499570.2:n.*1124G>C
|
|
ENST00000700202.2:c.9511G>C
|
ENSP00000514856.2:p.Asp3171His
|
|
ENST00000700202.1:c.1978G>C
|
ENSP00000514856.1:p.Asp660His
|
|
ENST00000700203.1:n.1689G>C
|
|
|
ENST00000380152.8:c.9562G>C
MANE Select
|
ENSP00000369497.3:p.Asp3188His
|
|
ENST00000544455.6:c.9562G>C
|
ENSP00000439902.1:p.Asp3188His
|
|
ENST00000614259.2:c.9570G>C
|
ENSP00000506251.1:n.9570G>C
|
|
ENST00000665585.1:c.2440G>C
|
|
|
ENST00000680887.1:c.9562G>C
|
ENSP00000505508.1:p.Asp3188His
|
|
ENST00000380152.7:c.9562G>C
|
ENSP00000369497.3:p.Asp3188His
|
|
ENST00000470094.1:c.645G>C
|
|
|
ENST00000533776.1:n.150G>C
|
|
|
ENST00000544455.5:c.9562G>C
|
ENSP00000439902.1:p.Asp3188His
|
|
NM_000059.3:c.9562G>C , LRG_293t1:c.9562G>C
|
NP_000050.2:p.Asp3188His
|
|
XM_011535203.1:c.9562G>C
|
XP_011533505.1:p.Asp3188His
|
|
XM_011535204.1:c.9466G>C
|
XP_011533506.1:p.Asp3156His
|
|
NM_000059.4:c.9562G>C
MANE Select
|
NP_000050.3:p.Asp3188His
|
|