ENST00000636937.2:c.2227G>C
|
ENSP00000516154.1:p.Asp743His
|
|
ENST00000268124.11:c.2227G>C
MANE Select
|
ENSP00000268124.5:p.Asp743His
|
|
ENST00000530292.3:c.1828G>C
|
ENSP00000432885.2:p.Asp610His
|
|
ENST00000635986.2:c.2227G>C
|
ENSP00000490653.2:p.Asp743His
|
|
ENST00000636774.1:c.*794G>C
|
ENSP00000489799.1:n.*794G>C
|
|
ENST00000637238.1:c.924G>C
|
ENSP00000490756.1:n.924G>C
|
|
ENST00000637264.1:c.1299G>C
|
|
|
ENST00000666746.1:c.1804G>C
|
|
|
ENST00000670281.1:c.547G>C
|
ENSP00000499709.1:p.Asp183His
|
|
ENST00000672071.1:n.2425G>C
|
|
|
ENST00000672923.2:n.2330G>C
|
|
|
ENST00000268124.9:c.2227G>C
|
ENSP00000268124.5:p.Asp743His
|
|
ENST00000442287.6:c.2227G>C
|
ENSP00000399851.2:p.Asp743His
|
|
ENST00000526314.2:c.539+373G>C
|
|
|
ENST00000526398.1:c.376G>C
|
|
|
ENST00000532584.5:n.429G>C
|
|
|
ENST00000631044.2:c.*1651G>C
|
ENSP00000486730.1:n.*1651G>C
|
|
NM_001126131.1:c.2227G>C
|
NP_001119603.1:p.Asp743His
|
|
NM_002693.2:c.2227G>C
|
NP_002684.1:p.Asp743His
|
|
NM_001126131.2:c.2227G>C
|
NP_001119603.1:p.Asp743His
|
|
NM_002693.3:c.2227G>C
MANE Select
|
NP_002684.1:p.Asp743His
|
|