ENST00000645828.1:n.2746C>A
|
|
|
ENST00000651671.1:c.4939C>A
MANE Select
|
ENSP00000498587.1:p.Gln1647Lys
|
|
ENST00000679595.1:c.4939C>A
|
ENSP00000506241.1:p.Gln1647Lys
|
|
ENST00000680133.1:c.4825C>A
|
ENSP00000505319.1:p.Gln1609Lys
|
|
ENST00000680218.1:c.4819C>A
|
ENSP00000505339.1:p.Gln1607Lys
|
|
ENST00000680668.1:c.4825C>A
|
ENSP00000506336.1:p.Gln1609Lys
|
|
ENST00000680778.1:c.2536C>A
|
ENSP00000506033.1:p.Gln846Lys
|
|
ENST00000680924.1:c.*2339C>A
|
ENSP00000506031.1:n.*2339C>A
|
|
ENST00000681135.1:c.*2548C>A
|
ENSP00000506636.1:n.*2548C>A
|
|
ENST00000681298.1:n.1752C>A
|
|
|
ENST00000681454.1:c.*4175C>A
|
ENSP00000505763.1:n.*4175C>A
|
|
ENST00000277541.6:c.4939C>A
|
ENSP00000277541.6:p.Gln1647Lys
|
|
ENST00000494783.1:n.94C>A
|
|
|
NM_017617.3:c.4939C>A
|
NP_060087.3:p.Gln1647Lys
|
|
XM_011518717.1:c.4240C>A
|
XP_011517019.1:p.Gln1414Lys
|
|
NM_017617.5:c.4939C>A
MANE Select
|
NP_060087.3:p.Gln1647Lys
|
|
XM_011518717.2:c.4216C>A
|
XP_011517019.2:p.Gln1406Lys
|
|