ENST00000636937.2:c.1489C>A
|
ENSP00000516154.1:p.Gln497Lys
|
|
ENST00000268124.11:c.1489C>A
MANE Select
|
ENSP00000268124.5:p.Gln497Lys
|
|
ENST00000530292.3:c.1090C>A
|
ENSP00000432885.2:p.Gln364Lys
|
|
ENST00000635986.2:c.1489C>A
|
ENSP00000490653.2:p.Gln497Lys
|
|
ENST00000636774.1:c.*56C>A
|
ENSP00000489799.1:n.*56C>A
|
|
ENST00000637238.1:c.226C>A
|
ENSP00000490756.1:p.Gln76Lys
|
|
ENST00000637264.1:c.561C>A
|
|
|
ENST00000666746.1:c.1066C>A
|
|
|
ENST00000672071.1:n.1687C>A
|
|
|
ENST00000672923.2:n.1592C>A
|
|
|
ENST00000268124.9:c.1489C>A
|
ENSP00000268124.5:p.Gln497Lys
|
|
ENST00000442287.6:c.1489C>A
|
ENSP00000399851.2:p.Gln497Lys
|
|
ENST00000631044.2:c.*872C>A
|
ENSP00000486730.1:n.*872C>A
|
|
NM_001126131.1:c.1489C>A
|
NP_001119603.1:p.Gln497Lys
|
|
NM_002693.2:c.1489C>A
|
NP_002684.1:p.Gln497Lys
|
|
NM_001126131.2:c.1489C>A
|
NP_001119603.1:p.Gln497Lys
|
|
NM_002693.3:c.1489C>A
MANE Select
|
NP_002684.1:p.Gln497Lys
|
|