ENST00000645828.1:n.2469C>A
|
|
|
ENST00000651671.1:c.4662C>A
MANE Select
|
ENSP00000498587.1:p.Cys1554Ter
|
|
ENST00000679595.1:c.4662C>A
|
ENSP00000506241.1:p.Cys1554Ter
|
|
ENST00000680133.1:c.4548C>A
|
ENSP00000505319.1:p.Cys1516Ter
|
|
ENST00000680218.1:c.4542C>A
|
ENSP00000505339.1:p.Cys1514Ter
|
|
ENST00000680668.1:c.4548C>A
|
ENSP00000506336.1:p.Cys1516Ter
|
|
ENST00000680778.1:c.2259C>A
|
ENSP00000506033.1:p.Cys753Ter
|
|
ENST00000680924.1:c.*2062C>A
|
ENSP00000506031.1:n.*2062C>A
|
|
ENST00000681135.1:c.*2271C>A
|
ENSP00000506636.1:n.*2271C>A
|
|
ENST00000681298.1:n.1475C>A
|
|
|
ENST00000681454.1:c.*3898C>A
|
ENSP00000505763.1:n.*3898C>A
|
|
ENST00000277541.6:c.4662C>A
|
ENSP00000277541.6:p.Cys1554Ter
|
|
NM_017617.3:c.4662C>A
|
NP_060087.3:p.Cys1554Ter
|
|
XM_011518717.1:c.3963C>A
|
XP_011517019.1:p.Cys1321Ter
|
|
NM_017617.5:c.4662C>A
MANE Select
|
NP_060087.3:p.Cys1554Ter
|
|
XM_011518717.2:c.3939C>A
|
XP_011517019.2:p.Cys1313Ter
|
|