ENST00000636937.2:c.1713A>T
|
ENSP00000516154.1:p.Gly571=
|
|
ENST00000268124.11:c.1713A>T
MANE Select
|
ENSP00000268124.5:p.Gly571=
|
|
ENST00000530292.3:c.1314A>T
|
ENSP00000432885.2:p.Gly438=
|
|
ENST00000635986.2:c.1713A>T
|
ENSP00000490653.2:p.Gly571=
|
|
ENST00000636774.1:c.*280A>T
|
ENSP00000489799.1:n.*280A>T
|
|
ENST00000637238.1:c.450A>T
|
ENSP00000490756.1:p.Gly150=
|
|
ENST00000637264.1:c.785A>T
|
|
|
ENST00000666746.1:c.1290A>T
|
|
|
ENST00000670281.1:c.33A>T
|
ENSP00000499709.1:p.Gly11=
|
|
ENST00000672071.1:n.1911A>T
|
|
|
ENST00000672923.2:n.1816A>T
|
|
|
ENST00000268124.9:c.1713A>T
|
ENSP00000268124.5:p.Gly571=
|
|
ENST00000442287.6:c.1713A>T
|
ENSP00000399851.2:p.Gly571=
|
|
ENST00000526314.2:c.95A>T
|
|
|
ENST00000631044.2:c.*1096A>T
|
ENSP00000486730.1:n.*1096A>T
|
|
NM_001126131.1:c.1713A>T
|
NP_001119603.1:p.Gly571=
|
|
NM_002693.2:c.1713A>T
|
NP_002684.1:p.Gly571=
|
|
NM_001126131.2:c.1713A>T
|
NP_001119603.1:p.Gly571=
|
|
NM_002693.3:c.1713A>T
MANE Select
|
NP_002684.1:p.Gly571=
|
|