ENST00000295497.13:c.311T>A
|
ENSP00000295497.7:p.Leu104His
|
|
ENST00000444394.7:c.311T>A
|
ENSP00000411911.2:p.Leu104His
|
|
ENST00000295497.12:c.311T>A
|
ENSP00000295497.7:p.Leu104His
|
|
ENST00000409089.7:c.11T>A
|
ENSP00000386322.3:p.Leu4His
|
|
ENST00000409900.9:c.686T>A
MANE Select
|
ENSP00000386741.4:p.Leu229His
|
|
ENST00000413882.6:c.140T>A
|
ENSP00000410496.2:p.Leu47His
|
|
ENST00000425395.6:c.*133T>A
|
ENSP00000405270.2:n.*133T>A
|
|
ENST00000443238.6:c.164T>A
|
ENSP00000409798.2:p.Leu55His
|
|
ENST00000444394.6:c.311T>A
|
ENSP00000411911.2:p.Leu104His
|
|
ENST00000444573.2:c.530T>A
|
ENSP00000392603.2:p.Leu177His
|
|
ENST00000488080.6:n.329T>A
|
|
|
ENST00000650731.1:c.11T>A
|
ENSP00000499146.1:p.Leu4His
|
|
ENST00000650938.1:c.210T>A
|
|
|
ENST00000651246.1:c.278T>A
|
ENSP00000498484.1:p.Leu93His
|
|
ENST00000651373.1:c.200T>A
|
ENSP00000499174.1:p.Leu67His
|
|
ENST00000651501.1:c.*133T>A
|
ENSP00000498894.1:n.*133T>A
|
|
ENST00000651717.1:c.253-11978T>A
|
ENSP00000499124.1:n.253-11978T>A
|
|
ENST00000652036.1:c.311T>A
|
ENSP00000499139.1:p.Leu104His
|
|
ENST00000652154.1:n.584T>A
|
|
|
ENST00000295497.11:c.311T>A
|
ENSP00000295497.7:p.Leu104His
|
|
ENST00000409089.6:c.11T>A
|
ENSP00000386322.2:p.Leu4His
|
|
ENST00000409156.7:c.608T>A
|
ENSP00000386470.3:p.Leu203His
|
|
ENST00000409597.5:c.134T>A
|
ENSP00000386469.1:p.Leu45His
|
|
ENST00000409900.7:c.686T>A
|
ENSP00000386741.3:p.Leu229His
|
|
ENST00000413882.5:c.140T>A
|
ENSP00000410496.1:p.Leu47His
|
|
ENST00000425395.5:c.*237T>A
|
ENSP00000405270.1:n.*237T>A
|
|
ENST00000443238.5:c.164T>A
|
ENSP00000409798.1:p.Leu55His
|
|
ENST00000444394.5:c.11T>A
|
ENSP00000411911.1:p.Leu4His
|
|
ENST00000444573.1:c.311T>A
|
ENSP00000392603.1:p.Leu104His
|
|
ENST00000485882.1:n.145T>A
|
|
|
ENST00000488080.5:n.537T>A
|
|
|
NM_001025201.3:c.608T>A
|
NP_001020372.2:p.Leu203His
|
|
NM_001206602.1:c.311T>A
|
NP_001193531.1:p.Leu104His
|
|
NM_001822.5:c.686T>A
|
NP_001813.1:p.Leu229His
|
|
NR_038133.1:n.552T>A
|
|
|
NM_001025201.4:c.608T>A
|
NP_001020372.2:p.Leu203His
|
|
NM_001206602.2:c.311T>A
|
NP_001193531.1:p.Leu104His
|
|
NM_001371513.1:c.686T>A
|
NP_001358442.1:p.Leu229His
|
|
NM_001371514.1:c.737T>A
|
NP_001358443.1:p.Leu246His
|
|
NM_001822.7:c.686T>A
MANE Select
|
NP_001813.1:p.Leu229His
|
|
NR_038133.2:n.554T>A
|
|
|