ENST00000256906.5:c.699T>G
MANE Select
|
ENSP00000256906.4:p.Ser233=
|
|
ENST00000256906.4:c.699T>G
|
ENSP00000256906.4:p.Ser233=
|
|
ENST00000426880.2:c.435T>G
|
ENSP00000402526.2:p.Ser145=
|
|
NM_001143828.1:c.435T>G
|
NP_001137300.1:p.Ser145=
|
|
NM_001160166.1:c.*331T>G
|
NP_001153638.1:n.*331T>G
|
|
NM_021624.3:c.699T>G
|
NP_067637.2:p.Ser233=
|
|
XM_011526133.1:c.357+8137T>G
|
XP_011524435.1:n.357+8137T>G
|
|
NM_021624.4:c.699T>G
MANE Select
|
NP_067637.2:p.Ser233=
|
|
NM_001143828.2:c.435T>G
|
NP_001137300.1:p.Ser145=
|
|
NM_001160166.2:c.*331T>G
|
NP_001153638.1:n.*331T>G
|
|