ENST00000645828.1:n.2743G>T
|
|
|
ENST00000651671.1:c.4936G>T
MANE Select
|
ENSP00000498587.1:p.Gly1646Cys
|
|
ENST00000679595.1:c.4936G>T
|
ENSP00000506241.1:p.Gly1646Cys
|
|
ENST00000680133.1:c.4822G>T
|
ENSP00000505319.1:p.Gly1608Cys
|
|
ENST00000680218.1:c.4816G>T
|
ENSP00000505339.1:p.Gly1606Cys
|
|
ENST00000680668.1:c.4822G>T
|
ENSP00000506336.1:p.Gly1608Cys
|
|
ENST00000680778.1:c.2533G>T
|
ENSP00000506033.1:p.Gly845Cys
|
|
ENST00000680924.1:c.*2336G>T
|
ENSP00000506031.1:n.*2336G>T
|
|
ENST00000681135.1:c.*2545G>T
|
ENSP00000506636.1:n.*2545G>T
|
|
ENST00000681298.1:n.1749G>T
|
|
|
ENST00000681454.1:c.*4172G>T
|
ENSP00000505763.1:n.*4172G>T
|
|
ENST00000277541.6:c.4936G>T
|
ENSP00000277541.6:p.Gly1646Cys
|
|
ENST00000494783.1:n.91G>T
|
|
|
NM_017617.3:c.4936G>T
|
NP_060087.3:p.Gly1646Cys
|
|
XM_011518717.1:c.4237G>T
|
XP_011517019.1:p.Gly1413Cys
|
|
NM_017617.5:c.4936G>T
MANE Select
|
NP_060087.3:p.Gly1646Cys
|
|
XM_011518717.2:c.4213G>T
|
XP_011517019.2:p.Gly1405Cys
|
|