ENST00000645828.1:n.2746C>G
|
|
|
ENST00000651671.1:c.4939C>G
MANE Select
|
ENSP00000498587.1:p.Gln1647Glu
|
|
ENST00000679595.1:c.4939C>G
|
ENSP00000506241.1:p.Gln1647Glu
|
|
ENST00000680133.1:c.4825C>G
|
ENSP00000505319.1:p.Gln1609Glu
|
|
ENST00000680218.1:c.4819C>G
|
ENSP00000505339.1:p.Gln1607Glu
|
|
ENST00000680668.1:c.4825C>G
|
ENSP00000506336.1:p.Gln1609Glu
|
|
ENST00000680778.1:c.2536C>G
|
ENSP00000506033.1:p.Gln846Glu
|
|
ENST00000680924.1:c.*2339C>G
|
ENSP00000506031.1:n.*2339C>G
|
|
ENST00000681135.1:c.*2548C>G
|
ENSP00000506636.1:n.*2548C>G
|
|
ENST00000681298.1:n.1752C>G
|
|
|
ENST00000681454.1:c.*4175C>G
|
ENSP00000505763.1:n.*4175C>G
|
|
ENST00000277541.6:c.4939C>G
|
ENSP00000277541.6:p.Gln1647Glu
|
|
ENST00000494783.1:n.94C>G
|
|
|
NM_017617.3:c.4939C>G
|
NP_060087.3:p.Gln1647Glu
|
|
XM_011518717.1:c.4240C>G
|
XP_011517019.1:p.Gln1414Glu
|
|
NM_017617.5:c.4939C>G
MANE Select
|
NP_060087.3:p.Gln1647Glu
|
|
XM_011518717.2:c.4216C>G
|
XP_011517019.2:p.Gln1406Glu
|
|