ENST00000407445.8:c.87G>T
|
ENSP00000385729.3:p.Glu29Asp
|
|
ENST00000491937.6:n.133G>T
|
|
|
ENST00000645674.2:c.87G>T
MANE Select
|
ENSP00000496757.1:p.Glu29Asp
|
|
ENST00000646909.1:c.87G>T
|
ENSP00000496654.1:p.Glu29Asp
|
|
ENST00000647131.1:c.87G>T
|
ENSP00000494995.1:p.Glu29Asp
|
|
ENST00000304921.9:c.87G>T
|
ENSP00000339095.4:p.Glu29Asp
|
|
ENST00000403564.5:c.87G>T
|
ENSP00000385018.1:p.Glu29Asp
|
|
ENST00000406376.1:c.87G>T
|
ENSP00000385286.1:p.Glu29Asp
|
|
ENST00000407445.7:c.87G>T
|
ENSP00000385729.3:p.Glu29Asp
|
|
ENST00000462576.5:n.372G>T
|
|
|
ENST00000479123.1:n.64G>T
|
|
|
ENST00000481006.1:n.339G>T
|
|
|
ENST00000491937.5:n.352G>T
|
|
|
NM_001011.3:c.87G>T
|
NP_001002.1:p.Glu29Asp
|
|
NM_001011.4:c.87G>T
MANE Select
|
NP_001002.1:p.Glu29Asp
|
|