ENST00000636937.2:c.2222A>T
|
ENSP00000516154.1:p.Asp741Val
|
|
ENST00000268124.11:c.2222A>T
MANE Select
|
ENSP00000268124.5:p.Asp741Val
|
|
ENST00000530292.3:c.1823A>T
|
ENSP00000432885.2:p.Asp608Val
|
|
ENST00000635986.2:c.2222A>T
|
ENSP00000490653.2:p.Asp741Val
|
|
ENST00000636774.1:c.*789A>T
|
ENSP00000489799.1:n.*789A>T
|
|
ENST00000637238.1:c.919A>T
|
ENSP00000490756.1:n.919A>T
|
|
ENST00000637264.1:c.1294A>T
|
|
|
ENST00000666746.1:c.1799A>T
|
|
|
ENST00000670281.1:c.542A>T
|
ENSP00000499709.1:p.Asp181Val
|
|
ENST00000672071.1:n.2420A>T
|
|
|
ENST00000672923.2:n.2325A>T
|
|
|
ENST00000268124.9:c.2222A>T
|
ENSP00000268124.5:p.Asp741Val
|
|
ENST00000442287.6:c.2222A>T
|
ENSP00000399851.2:p.Asp741Val
|
|
ENST00000526314.2:c.539+368A>T
|
|
|
ENST00000526398.1:c.371A>T
|
|
|
ENST00000532584.5:n.424A>T
|
|
|
ENST00000631044.2:c.*1646A>T
|
ENSP00000486730.1:n.*1646A>T
|
|
NM_001126131.1:c.2222A>T
|
NP_001119603.1:p.Asp741Val
|
|
NM_002693.2:c.2222A>T
|
NP_002684.1:p.Asp741Val
|
|
NM_001126131.2:c.2222A>T
|
NP_001119603.1:p.Asp741Val
|
|
NM_002693.3:c.2222A>T
MANE Select
|
NP_002684.1:p.Asp741Val
|
|