ENST00000636937.2:c.1826G>A
|
ENSP00000516154.1:p.Gly609Asp
|
|
ENST00000268124.11:c.1826G>A
MANE Select
|
ENSP00000268124.5:p.Gly609Asp
|
|
ENST00000530292.3:c.1427G>A
|
ENSP00000432885.2:p.Gly476Asp
|
|
ENST00000635986.2:c.1826G>A
|
ENSP00000490653.2:p.Gly609Asp
|
|
ENST00000636774.1:c.*393G>A
|
ENSP00000489799.1:n.*393G>A
|
|
ENST00000637238.1:c.563G>A
|
ENSP00000490756.1:p.Gly188Asp
|
|
ENST00000637264.1:c.898G>A
|
|
|
ENST00000666746.1:c.1403G>A
|
|
|
ENST00000670281.1:c.146G>A
|
ENSP00000499709.1:p.Gly49Asp
|
|
ENST00000672071.1:n.2024G>A
|
|
|
ENST00000672923.2:n.1929G>A
|
|
|
ENST00000268124.9:c.1826G>A
|
ENSP00000268124.5:p.Gly609Asp
|
|
ENST00000442287.6:c.1826G>A
|
ENSP00000399851.2:p.Gly609Asp
|
|
ENST00000526314.2:c.208G>A
|
|
|
ENST00000526398.1:c.15G>A
|
|
|
ENST00000532584.5:n.28G>A
|
|
|
ENST00000631044.2:c.*1209G>A
|
ENSP00000486730.1:n.*1209G>A
|
|
NM_001126131.1:c.1826G>A
|
NP_001119603.1:p.Gly609Asp
|
|
NM_002693.2:c.1826G>A
|
NP_002684.1:p.Gly609Asp
|
|
NM_001126131.2:c.1826G>A
|
NP_001119603.1:p.Gly609Asp
|
|
NM_002693.3:c.1826G>A
MANE Select
|
NP_002684.1:p.Gly609Asp
|
|