ENST00000645828.1:n.2633A>T
|
|
|
ENST00000651671.1:c.4826A>T
MANE Select
|
ENSP00000498587.1:p.Asp1609Val
|
|
ENST00000679595.1:c.4826A>T
|
ENSP00000506241.1:p.Asp1609Val
|
|
ENST00000680133.1:c.4712A>T
|
ENSP00000505319.1:p.Asp1571Val
|
|
ENST00000680218.1:c.4706A>T
|
ENSP00000505339.1:p.Asp1569Val
|
|
ENST00000680668.1:c.4712A>T
|
ENSP00000506336.1:p.Asp1571Val
|
|
ENST00000680778.1:c.2423A>T
|
ENSP00000506033.1:p.Asp808Val
|
|
ENST00000680924.1:c.*2226A>T
|
ENSP00000506031.1:n.*2226A>T
|
|
ENST00000681135.1:c.*2435A>T
|
ENSP00000506636.1:n.*2435A>T
|
|
ENST00000681298.1:n.1639A>T
|
|
|
ENST00000681454.1:c.*4062A>T
|
ENSP00000505763.1:n.*4062A>T
|
|
ENST00000277541.6:c.4826A>T
|
ENSP00000277541.6:p.Asp1609Val
|
|
NM_017617.3:c.4826A>T
|
NP_060087.3:p.Asp1609Val
|
|
XM_011518717.1:c.4127A>T
|
XP_011517019.1:p.Asp1376Val
|
|
NM_017617.5:c.4826A>T
MANE Select
|
NP_060087.3:p.Asp1609Val
|
|
XM_011518717.2:c.4103A>T
|
XP_011517019.2:p.Asp1368Val
|
|