ENST00000470094.2:c.*79G=
|
ENSP00000434898.2:n.*79G=
|
|
ENST00000528762.2:c.*923G=
|
ENSP00000433168.2:n.*923G=
|
|
ENST00000530893.7:c.9187G=
|
ENSP00000499438.2:p.Ala3063=
|
|
ENST00000665585.2:c.*1118G=
|
ENSP00000499570.2:n.*1118G=
|
|
ENST00000700202.2:c.9505G=
|
ENSP00000514856.2:p.Ala3169=
|
|
ENST00000700202.1:c.1972G=
|
ENSP00000514856.1:p.Ala658=
|
|
ENST00000700203.1:n.1683G=
|
|
|
ENST00000380152.8:c.9556G=
MANE Select
|
ENSP00000369497.3:p.Ala3186=
|
|
ENST00000544455.6:c.9556G=
|
ENSP00000439902.1:p.Ala3186=
|
|
ENST00000614259.2:c.9564G=
|
ENSP00000506251.1:n.9564G=
|
|
ENST00000665585.1:c.2434G=
|
|
|
ENST00000680887.1:c.9556G=
|
ENSP00000505508.1:p.Ala3186=
|
|
ENST00000380152.7:c.9556G=
|
ENSP00000369497.3:p.Ala3186=
|
|
ENST00000470094.1:c.639G=
|
|
|
ENST00000533776.1:n.144G=
|
|
|
ENST00000544455.5:c.9556G=
|
ENSP00000439902.1:p.Ala3186=
|
|
NM_000059.3:c.9556G= , LRG_293t1:c.9556G=
|
NP_000050.2:p.Ala3186=
|
|
XM_011535203.1:c.9556G=
|
XP_011533505.1:p.Ala3186=
|
|
XM_011535204.1:c.9460G=
|
XP_011533506.1:p.Ala3154=
|
|
NM_000059.4:c.9556G=
MANE Select
|
NP_000050.3:p.Ala3186=
|
|