ENST00000636937.2:c.3369T>A
|
ENSP00000516154.1:p.Phe1123Leu
|
|
ENST00000268124.11:c.3369T>A
MANE Select
|
ENSP00000268124.5:p.Phe1123Leu
|
|
ENST00000530292.3:c.2970T>A
|
ENSP00000432885.2:p.Phe990Leu
|
|
ENST00000635986.2:c.*439T>A
|
ENSP00000490653.2:n.*439T>A
|
|
ENST00000636774.1:c.*1936T>A
|
ENSP00000489799.1:n.*1936T>A
|
|
ENST00000637238.1:c.2178T>A
|
ENSP00000490756.1:n.2178T>A
|
|
ENST00000637264.1:c.2441T>A
|
|
|
ENST00000666746.1:c.2946T>A
|
|
|
ENST00000672071.1:n.3567T>A
|
|
|
ENST00000672695.1:n.546T>A
|
|
|
ENST00000672923.2:n.3369T>A
|
|
|
ENST00000268124.9:c.3369T>A
|
ENSP00000268124.5:p.Phe1123Leu
|
|
ENST00000442287.6:c.3369T>A
|
ENSP00000399851.2:p.Phe1123Leu
|
|
ENST00000530292.2:c.453T>A
|
ENSP00000432885.1:p.Phe151Leu
|
|
ENST00000631044.2:c.*2793T>A
|
ENSP00000486730.1:n.*2793T>A
|
|
NM_001126131.1:c.3369T>A
|
NP_001119603.1:p.Phe1123Leu
|
|
NM_002693.2:c.3369T>A
|
NP_002684.1:p.Phe1123Leu
|
|
NM_001126131.2:c.3369T>A
|
NP_001119603.1:p.Phe1123Leu
|
|
NM_002693.3:c.3369T>A
MANE Select
|
NP_002684.1:p.Phe1123Leu
|
|