ENST00000645828.1:n.2733C>G
|
|
|
ENST00000651671.1:c.4926C>G
MANE Select
|
ENSP00000498587.1:p.Asp1642Glu
|
|
ENST00000679595.1:c.4926C>G
|
ENSP00000506241.1:p.Asp1642Glu
|
|
ENST00000680133.1:c.4812C>G
|
ENSP00000505319.1:p.Asp1604Glu
|
|
ENST00000680218.1:c.4806C>G
|
ENSP00000505339.1:p.Asp1602Glu
|
|
ENST00000680668.1:c.4812C>G
|
ENSP00000506336.1:p.Asp1604Glu
|
|
ENST00000680778.1:c.2523C>G
|
ENSP00000506033.1:p.Asp841Glu
|
|
ENST00000680924.1:c.*2326C>G
|
ENSP00000506031.1:n.*2326C>G
|
|
ENST00000681135.1:c.*2535C>G
|
ENSP00000506636.1:n.*2535C>G
|
|
ENST00000681298.1:n.1739C>G
|
|
|
ENST00000681454.1:c.*4162C>G
|
ENSP00000505763.1:n.*4162C>G
|
|
ENST00000277541.6:c.4926C>G
|
ENSP00000277541.6:p.Asp1642Glu
|
|
ENST00000494783.1:n.81C>G
|
|
|
NM_017617.3:c.4926C>G
|
NP_060087.3:p.Asp1642Glu
|
|
XM_011518717.1:c.4227C>G
|
XP_011517019.1:p.Asp1409Glu
|
|
NM_017617.5:c.4926C>G
MANE Select
|
NP_060087.3:p.Asp1642Glu
|
|
XM_011518717.2:c.4203C>G
|
XP_011517019.2:p.Asp1401Glu
|
|