ENST00000651671.1:c.6059A>T
MANE Select
|
ENSP00000498587.1:p.Asp2020Val
|
|
ENST00000679595.1:c.*1099A>T
|
ENSP00000506241.1:n.*1099A>T
|
|
ENST00000679969.1:n.2540A>T
|
|
|
ENST00000680003.1:n.2391A>T
|
|
|
ENST00000680133.1:c.5945A>T
|
ENSP00000505319.1:p.Asp1982Val
|
|
ENST00000680218.1:c.5939A>T
|
ENSP00000505339.1:p.Asp1980Val
|
|
ENST00000680668.1:c.5945A>T
|
ENSP00000506336.1:p.Asp1982Val
|
|
ENST00000680778.1:c.3656A>T
|
ENSP00000506033.1:p.Asp1219Val
|
|
ENST00000680924.1:c.*3459A>T
|
ENSP00000506031.1:n.*3459A>T
|
|
ENST00000681135.1:c.*3668A>T
|
ENSP00000506636.1:n.*3668A>T
|
|
ENST00000681298.1:n.4164A>T
|
|
|
ENST00000681454.1:c.*5295A>T
|
ENSP00000505763.1:n.*5295A>T
|
|
ENST00000277541.6:c.6059A>T
|
ENSP00000277541.6:p.Asp2020Val
|
|
NM_017617.3:c.6059A>T
|
NP_060087.3:p.Asp2020Val
|
|
XM_011518717.1:c.5360A>T
|
XP_011517019.1:p.Asp1787Val
|
|
NM_017617.5:c.6059A>T
MANE Select
|
NP_060087.3:p.Asp2020Val
|
|
XM_011518717.2:c.5336A>T
|
XP_011517019.2:p.Asp1779Val
|
|