ENST00000636937.2:c.1936G>T
|
ENSP00000516154.1:p.Val646Phe
|
|
ENST00000268124.11:c.1936G>T
MANE Select
|
ENSP00000268124.5:p.Val646Phe
|
|
ENST00000530292.3:c.1537G>T
|
ENSP00000432885.2:p.Val513Phe
|
|
ENST00000635986.2:c.1936G>T
|
ENSP00000490653.2:p.Val646Phe
|
|
ENST00000636774.1:c.*503G>T
|
ENSP00000489799.1:n.*503G>T
|
|
ENST00000637238.1:c.646+27G>T
|
ENSP00000490756.1:n.646+27G>T
|
|
ENST00000637264.1:c.1008G>T
|
|
|
ENST00000666746.1:c.1513G>T
|
|
|
ENST00000670281.1:c.256G>T
|
ENSP00000499709.1:p.Val86Phe
|
|
ENST00000672071.1:n.2134G>T
|
|
|
ENST00000672923.2:n.2039G>T
|
|
|
ENST00000268124.9:c.1936G>T
|
ENSP00000268124.5:p.Val646Phe
|
|
ENST00000442287.6:c.1936G>T
|
ENSP00000399851.2:p.Val646Phe
|
|
ENST00000526314.2:c.318G>T
|
|
|
ENST00000526398.1:c.125G>T
|
|
|
ENST00000526573.1:n.22G>T
|
|
|
ENST00000532584.5:n.138G>T
|
|
|
ENST00000631044.2:c.*1319G>T
|
ENSP00000486730.1:n.*1319G>T
|
|
NM_001126131.1:c.1936G>T
|
NP_001119603.1:p.Val646Phe
|
|
NM_002693.2:c.1936G>T
|
NP_002684.1:p.Val646Phe
|
|
NM_001126131.2:c.1936G>T
|
NP_001119603.1:p.Val646Phe
|
|
NM_002693.3:c.1936G>T
MANE Select
|
NP_002684.1:p.Val646Phe
|
|