ENST00000645828.1:n.2675A>G
|
|
|
ENST00000651671.1:c.4868A>G
MANE Select
|
ENSP00000498587.1:p.Glu1623Gly
|
|
ENST00000679595.1:c.4868A>G
|
ENSP00000506241.1:p.Glu1623Gly
|
|
ENST00000680133.1:c.4754A>G
|
ENSP00000505319.1:p.Glu1585Gly
|
|
ENST00000680218.1:c.4748A>G
|
ENSP00000505339.1:p.Glu1583Gly
|
|
ENST00000680668.1:c.4754A>G
|
ENSP00000506336.1:p.Glu1585Gly
|
|
ENST00000680778.1:c.2465A>G
|
ENSP00000506033.1:p.Glu822Gly
|
|
ENST00000680924.1:c.*2268A>G
|
ENSP00000506031.1:n.*2268A>G
|
|
ENST00000681135.1:c.*2477A>G
|
ENSP00000506636.1:n.*2477A>G
|
|
ENST00000681298.1:n.1681A>G
|
|
|
ENST00000681454.1:c.*4104A>G
|
ENSP00000505763.1:n.*4104A>G
|
|
ENST00000277541.6:c.4868A>G
|
ENSP00000277541.6:p.Glu1623Gly
|
|
ENST00000494783.1:n.23A>G
|
|
|
NM_017617.3:c.4868A>G
|
NP_060087.3:p.Glu1623Gly
|
|
XM_011518717.1:c.4169A>G
|
XP_011517019.1:p.Glu1390Gly
|
|
NM_017617.5:c.4868A>G
MANE Select
|
NP_060087.3:p.Glu1623Gly
|
|
XM_011518717.2:c.4145A>G
|
XP_011517019.2:p.Glu1382Gly
|
|