ENST00000409900.9:c.475A>T
MANE Select
|
ENSP00000386741.4:p.Lys159Ter
|
|
ENST00000425395.6:c.105-30957A>T
|
ENSP00000405270.2:n.105-30957A>T
|
|
ENST00000444573.2:c.319A>T
|
ENSP00000392603.2:p.Lys107Ter
|
|
ENST00000451799.2:c.319A>T
|
ENSP00000416316.2:p.Lys107Ter
|
|
ENST00000469597.2:c.*123A>T
|
ENSP00000498417.1:n.*123A>T
|
|
ENST00000488080.6:n.115-2049A>T
|
|
|
ENST00000650734.1:c.*375A>T
|
ENSP00000498742.1:n.*375A>T
|
|
ENST00000650770.1:c.*389A>T
|
ENSP00000499036.1:n.*389A>T
|
|
ENST00000651063.1:n.526A>T
|
|
|
ENST00000651246.1:c.67A>T
|
ENSP00000498484.1:p.Lys23Ter
|
|
ENST00000651315.1:c.67A>T
|
ENSP00000498692.1:p.Lys23Ter
|
|
ENST00000651373.1:c.67A>T
|
ENSP00000499174.1:p.Lys23Ter
|
|
ENST00000651501.1:c.105-30957A>T
|
ENSP00000498894.1:n.105-30957A>T
|
|
ENST00000651580.1:c.319A>T
|
ENSP00000498631.1:p.Lys107Ter
|
|
ENST00000651599.1:c.319A>T
|
ENSP00000498535.1:p.Lys107Ter
|
|
ENST00000651803.1:c.*389A>T
|
ENSP00000499007.1:n.*389A>T
|
|
ENST00000651971.1:c.*275A>T
|
ENSP00000499035.1:n.*275A>T
|
|
ENST00000652154.1:n.451A>T
|
|
|
ENST00000652208.1:c.319A>T
|
ENSP00000498475.1:p.Lys107Ter
|
|
ENST00000652434.1:c.436A>T
|
ENSP00000498549.1:p.Lys146Ter
|
|
ENST00000652437.1:n.618A>T
|
|
|
ENST00000652674.1:c.67A>T
|
ENSP00000498599.1:p.Lys23Ter
|
|
ENST00000652734.1:n.372A>T
|
|
|
ENST00000652756.1:c.319A>T
|
ENSP00000498281.1:p.Lys107Ter
|
|
ENST00000652768.1:n.367A>T
|
|
|
ENST00000409156.7:c.475A>T
|
ENSP00000386470.3:p.Lys159Ter
|
|
ENST00000409900.7:c.475A>T
|
ENSP00000386741.3:p.Lys159Ter
|
|
ENST00000425395.5:c.*101-30957A>T
|
ENSP00000405270.1:n.*101-30957A>T
|
|
ENST00000469597.1:n.580A>T
|
|
|
ENST00000481174.1:n.28A>T
|
|
|
ENST00000488080.5:n.401-30957A>T
|
|
|
ENST00000490654.1:n.450A>T
|
|
|
NM_001025201.3:c.475A>T
|
NP_001020372.2:p.Lys159Ter
|
|
NM_001822.5:c.475A>T
|
NP_001813.1:p.Lys159Ter
|
|
NR_038133.1:n.416-30957A>T
|
|
|
NM_001025201.4:c.475A>T
|
NP_001020372.2:p.Lys159Ter
|
|
NM_001371513.1:c.475A>T
|
NP_001358442.1:p.Lys159Ter
|
|
NM_001371514.1:c.526A>T
|
NP_001358443.1:p.Lys176Ter
|
|
NM_001822.7:c.475A>T
MANE Select
|
NP_001813.1:p.Lys159Ter
|
|
NR_038133.2:n.418-30957A>T
|
|
|