ENST00000636937.2:c.1894G>T
|
ENSP00000516154.1:p.Ala632Ser
|
|
ENST00000268124.11:c.1894G>T
MANE Select
|
ENSP00000268124.5:p.Ala632Ser
|
|
ENST00000530292.3:c.1495G>T
|
ENSP00000432885.2:p.Ala499Ser
|
|
ENST00000635986.2:c.1894G>T
|
ENSP00000490653.2:p.Ala632Ser
|
|
ENST00000636774.1:c.*461G>T
|
ENSP00000489799.1:n.*461G>T
|
|
ENST00000637238.1:c.631G>T
|
ENSP00000490756.1:p.Ala211Ser
|
|
ENST00000637264.1:c.966G>T
|
|
|
ENST00000666746.1:c.1471G>T
|
|
|
ENST00000670281.1:c.214G>T
|
ENSP00000499709.1:p.Ala72Ser
|
|
ENST00000672071.1:n.2092G>T
|
|
|
ENST00000672923.2:n.1997G>T
|
|
|
ENST00000268124.9:c.1894G>T
|
ENSP00000268124.5:p.Ala632Ser
|
|
ENST00000442287.6:c.1894G>T
|
ENSP00000399851.2:p.Ala632Ser
|
|
ENST00000526314.2:c.276G>T
|
|
|
ENST00000526398.1:c.83G>T
|
|
|
ENST00000532584.5:n.96G>T
|
|
|
ENST00000631044.2:c.*1277G>T
|
ENSP00000486730.1:n.*1277G>T
|
|
NM_001126131.1:c.1894G>T
|
NP_001119603.1:p.Ala632Ser
|
|
NM_002693.2:c.1894G>T
|
NP_002684.1:p.Ala632Ser
|
|
NM_001126131.2:c.1894G>T
|
NP_001119603.1:p.Ala632Ser
|
|
NM_002693.3:c.1894G>T
MANE Select
|
NP_002684.1:p.Ala632Ser
|
|