ENST00000636937.2:c.3575A>T
|
ENSP00000516154.1:p.Glu1192Val
|
|
ENST00000268124.11:c.3575A>T
MANE Select
|
ENSP00000268124.5:p.Glu1192Val
|
|
ENST00000530292.3:c.3275A>T
|
ENSP00000432885.2:n.3275A>T
|
|
ENST00000635986.2:c.*645A>T
|
ENSP00000490653.2:n.*645A>T
|
|
ENST00000636774.1:c.*2179A>T
|
ENSP00000489799.1:n.*2179A>T
|
|
ENST00000637042.1:n.99A>T
|
|
|
ENST00000637238.1:c.2483A>T
|
ENSP00000490756.1:n.2483A>T
|
|
ENST00000637264.1:c.2587A>T
|
|
|
ENST00000666746.1:c.3152A>T
|
|
|
ENST00000672071.1:n.4777A>T
|
|
|
ENST00000672695.1:n.1354A>T
|
|
|
ENST00000672923.2:n.3575A>T
|
|
|
ENST00000268124.9:c.3575A>T
|
ENSP00000268124.5:p.Glu1192Val
|
|
ENST00000442287.6:c.3575A>T
|
ENSP00000399851.2:p.Glu1192Val
|
|
ENST00000526671.1:n.385A>T
|
|
|
ENST00000530292.2:c.758A>T
|
ENSP00000432885.1:n.758A>T
|
|
ENST00000631044.2:c.*2999A>T
|
ENSP00000486730.1:n.*2999A>T
|
|
NM_001126131.1:c.3575A>T
|
NP_001119603.1:p.Glu1192Val
|
|
NM_002693.2:c.3575A>T
|
NP_002684.1:p.Glu1192Val
|
|
NM_001126131.2:c.3575A>T
|
NP_001119603.1:p.Glu1192Val
|
|
NM_002693.3:c.3575A>T
MANE Select
|
NP_002684.1:p.Glu1192Val
|
|