ENST00000360215.3:c.552C>G
MANE Select
|
ENSP00000353346.1:p.Leu184=
|
|
ENST00000496656.2:n.331C>G
|
|
|
ENST00000651132.1:c.552C>G
|
ENSP00000498322.1:p.Leu184=
|
|
ENST00000651676.1:c.552C>G
|
ENSP00000498699.1:p.Leu184=
|
|
ENST00000651994.1:c.*70-4752C>G
|
ENSP00000498310.1:n.*70-4752C>G
|
|
ENST00000652718.1:c.384C>G
|
ENSP00000498866.1:p.Leu128=
|
|
ENST00000360215.2:c.552C>G
|
ENSP00000353346.1:p.Leu184=
|
|
ENST00000496656.1:n.331C>G
|
|
|
NM_182548.3:c.552C>G
|
NP_872354.1:p.Leu184=
|
|
XM_011514403.1:c.552C>G
|
XP_011512705.1:p.Leu184=
|
|
NM_182548.4:c.552C>G
MANE Select
|
NP_872354.1:p.Leu184=
|
|