ENST00000645828.1:n.2715G>C
|
|
|
ENST00000651671.1:c.4908G>C
MANE Select
|
ENSP00000498587.1:p.Glu1636Asp
|
|
ENST00000679595.1:c.4908G>C
|
ENSP00000506241.1:p.Glu1636Asp
|
|
ENST00000680133.1:c.4794G>C
|
ENSP00000505319.1:p.Glu1598Asp
|
|
ENST00000680218.1:c.4788G>C
|
ENSP00000505339.1:p.Glu1596Asp
|
|
ENST00000680668.1:c.4794G>C
|
ENSP00000506336.1:p.Glu1598Asp
|
|
ENST00000680778.1:c.2505G>C
|
ENSP00000506033.1:p.Glu835Asp
|
|
ENST00000680924.1:c.*2308G>C
|
ENSP00000506031.1:n.*2308G>C
|
|
ENST00000681135.1:c.*2517G>C
|
ENSP00000506636.1:n.*2517G>C
|
|
ENST00000681298.1:n.1721G>C
|
|
|
ENST00000681454.1:c.*4144G>C
|
ENSP00000505763.1:n.*4144G>C
|
|
ENST00000277541.6:c.4908G>C
|
ENSP00000277541.6:p.Glu1636Asp
|
|
ENST00000494783.1:n.63G>C
|
|
|
NM_017617.3:c.4908G>C
|
NP_060087.3:p.Glu1636Asp
|
|
XM_011518717.1:c.4209G>C
|
XP_011517019.1:p.Glu1403Asp
|
|
NM_017617.5:c.4908G>C
MANE Select
|
NP_060087.3:p.Glu1636Asp
|
|
XM_011518717.2:c.4185G>C
|
XP_011517019.2:p.Glu1395Asp
|
|