ENST00000360215.3:c.576C>T
MANE Select
|
ENSP00000353346.1:p.Leu192=
|
|
ENST00000496656.2:n.355C>T
|
|
|
ENST00000651132.1:c.576C>T
|
ENSP00000498322.1:p.Leu192=
|
|
ENST00000651676.1:c.576C>T
|
ENSP00000498699.1:p.Leu192=
|
|
ENST00000651994.1:c.*70-4728C>T
|
ENSP00000498310.1:n.*70-4728C>T
|
|
ENST00000652718.1:c.408C>T
|
ENSP00000498866.1:p.Leu136=
|
|
ENST00000360215.2:c.576C>T
|
ENSP00000353346.1:p.Leu192=
|
|
ENST00000496656.1:n.355C>T
|
|
|
NM_182548.3:c.576C>T
|
NP_872354.1:p.Leu192=
|
|
XM_011514403.1:c.576C>T
|
XP_011512705.1:p.Leu192=
|
|
NM_182548.4:c.576C>T
MANE Select
|
NP_872354.1:p.Leu192=
|
|