ENST00000636937.2:c.1737G>T
|
ENSP00000516154.1:p.Arg579=
|
|
ENST00000268124.11:c.1737G>T
MANE Select
|
ENSP00000268124.5:p.Arg579=
|
|
ENST00000530292.3:c.1338G>T
|
ENSP00000432885.2:p.Arg446=
|
|
ENST00000635986.2:c.1737G>T
|
ENSP00000490653.2:p.Arg579=
|
|
ENST00000636774.1:c.*304G>T
|
ENSP00000489799.1:n.*304G>T
|
|
ENST00000637238.1:c.474G>T
|
ENSP00000490756.1:p.Arg158=
|
|
ENST00000637264.1:c.809G>T
|
|
|
ENST00000666746.1:c.1314G>T
|
|
|
ENST00000670281.1:c.57G>T
|
ENSP00000499709.1:p.Arg19=
|
|
ENST00000672071.1:n.1935G>T
|
|
|
ENST00000672923.2:n.1840G>T
|
|
|
ENST00000268124.9:c.1737G>T
|
ENSP00000268124.5:p.Arg579=
|
|
ENST00000442287.6:c.1737G>T
|
ENSP00000399851.2:p.Arg579=
|
|
ENST00000526314.2:c.119G>T
|
|
|
ENST00000631044.2:c.*1120G>T
|
ENSP00000486730.1:n.*1120G>T
|
|
NM_001126131.1:c.1737G>T
|
NP_001119603.1:p.Arg579=
|
|
NM_002693.2:c.1737G>T
|
NP_002684.1:p.Arg579=
|
|
NM_001126131.2:c.1737G>T
|
NP_001119603.1:p.Arg579=
|
|
NM_002693.3:c.1737G>T
MANE Select
|
NP_002684.1:p.Arg579=
|
|