ENST00000636937.2:c.1751C>T
|
ENSP00000516154.1:p.Ala584Val
|
|
ENST00000268124.11:c.1751C>T
MANE Select
|
ENSP00000268124.5:p.Ala584Val
|
|
ENST00000530292.3:c.1352C>T
|
ENSP00000432885.2:p.Ala451Val
|
|
ENST00000635986.2:c.1751C>T
|
ENSP00000490653.2:p.Ala584Val
|
|
ENST00000636774.1:c.*318C>T
|
ENSP00000489799.1:n.*318C>T
|
|
ENST00000637238.1:c.488C>T
|
ENSP00000490756.1:p.Ala163Val
|
|
ENST00000637264.1:c.823C>T
|
|
|
ENST00000666746.1:c.1328C>T
|
|
|
ENST00000670281.1:c.71C>T
|
ENSP00000499709.1:p.Ala24Val
|
|
ENST00000672071.1:n.1949C>T
|
|
|
ENST00000672923.2:n.1854C>T
|
|
|
ENST00000268124.9:c.1751C>T
|
ENSP00000268124.5:p.Ala584Val
|
|
ENST00000442287.6:c.1751C>T
|
ENSP00000399851.2:p.Ala584Val
|
|
ENST00000526314.2:c.133C>T
|
|
|
ENST00000631044.2:c.*1134C>T
|
ENSP00000486730.1:n.*1134C>T
|
|
NM_001126131.1:c.1751C>T
|
NP_001119603.1:p.Ala584Val
|
|
NM_002693.2:c.1751C>T
|
NP_002684.1:p.Ala584Val
|
|
NM_001126131.2:c.1751C>T
|
NP_001119603.1:p.Ala584Val
|
|
NM_002693.3:c.1751C>T
MANE Select
|
NP_002684.1:p.Ala584Val
|
|