ENST00000636937.2:c.2158-11G>A
|
ENSP00000516154.1:n.2158-11G>A
|
|
ENST00000268124.11:c.2158-11G>A
MANE Select
|
ENSP00000268124.5:n.2158-11G>A
|
|
ENST00000530292.3:c.1759-11G>A
|
ENSP00000432885.2:n.1759-11G>A
|
|
ENST00000635986.2:c.2158-11G>A
|
ENSP00000490653.2:n.2158-11G>A
|
|
ENST00000636774.1:c.*725-11G>A
|
ENSP00000489799.1:n.*725-11G>A
|
|
ENST00000637238.1:c.855-11G>A
|
ENSP00000490756.1:n.855-11G>A
|
|
ENST00000637264.1:c.1230-11G>A
|
|
|
ENST00000666746.1:c.1735-11G>A
|
|
|
ENST00000670281.1:c.478-11G>A
|
ENSP00000499709.1:n.478-11G>A
|
|
ENST00000672071.1:n.2356-11G>A
|
|
|
ENST00000672923.2:n.2261-11G>A
|
|
|
ENST00000268124.9:c.2158-11G>A
|
ENSP00000268124.5:n.2158-11G>A
|
|
ENST00000442287.6:c.2158-11G>A
|
ENSP00000399851.2:n.2158-11G>A
|
|
ENST00000526314.2:c.539+293G>A
|
|
|
ENST00000526398.1:c.307-11G>A
|
|
|
ENST00000526573.1:n.536G>A
|
|
|
ENST00000532584.5:n.360-11G>A
|
|
|
ENST00000533857.1:n.565G>A
|
|
|
ENST00000631044.2:c.*1571G>A
|
ENSP00000486730.1:n.*1571G>A
|
|
NM_001126131.1:c.2158-11G>A
|
NP_001119603.1:n.2158-11G>A
|
|
NM_002693.2:c.2158-11G>A
|
NP_002684.1:n.2158-11G>A
|
|
NM_001126131.2:c.2158-11G>A
|
NP_001119603.1:n.2158-11G>A
|
|
NM_002693.3:c.2158-11G>A
MANE Select
|
NP_002684.1:n.2158-11G>A
|
|