ENST00000651671.1:c.6519C>A
MANE Select
|
ENSP00000498587.1:p.Ala2173=
|
|
ENST00000679595.1:c.*1559C>A
|
ENSP00000506241.1:n.*1559C>A
|
|
ENST00000679969.1:n.3115C>A
|
|
|
ENST00000680003.1:n.2851C>A
|
|
|
ENST00000680133.1:c.6405C>A
|
ENSP00000505319.1:p.Ala2135=
|
|
ENST00000680218.1:c.6399C>A
|
ENSP00000505339.1:p.Ala2133=
|
|
ENST00000680668.1:c.6405C>A
|
ENSP00000506336.1:p.Ala2135=
|
|
ENST00000680778.1:c.4116C>A
|
ENSP00000506033.1:p.Ala1372=
|
|
ENST00000680924.1:c.*3919C>A
|
ENSP00000506031.1:n.*3919C>A
|
|
ENST00000681135.1:c.*4128C>A
|
ENSP00000506636.1:n.*4128C>A
|
|
ENST00000681298.1:n.4624C>A
|
|
|
ENST00000681454.1:c.*5755C>A
|
ENSP00000505763.1:n.*5755C>A
|
|
ENST00000277541.6:c.6519C>A
|
ENSP00000277541.6:p.Ala2173=
|
|
NM_017617.3:c.6519C>A
|
NP_060087.3:p.Ala2173=
|
|
XM_011518717.1:c.5820C>A
|
XP_011517019.1:p.Ala1940=
|
|
NM_017617.5:c.6519C>A
MANE Select
|
NP_060087.3:p.Ala2173=
|
|
XM_011518717.2:c.5796C>A
|
XP_011517019.2:p.Ala1932=
|
|