ENST00000269980.7:c.829G>C
MANE Select
|
ENSP00000269980.2:p.Glu277Gln
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ENST00000269980.6:c.829G>C
|
ENSP00000269980.2:p.Glu277Gln
|
|
ENST00000457836.6:c.763G>C
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ENSP00000416000.2:p.Glu255Gln
|
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ENST00000535632.5:n.458G>C
|
|
|
ENST00000540732.3:c.931G>C
|
ENSP00000443246.1:p.Glu311Gln
|
|
ENST00000542943.5:c.742G>C
|
ENSP00000440345.1:p.Glu248Gln
|
|
ENST00000545787.1:n.457G>C
|
|
|
ENST00000595085.5:c.829G>C
|
ENSP00000471150.2:p.Glu277Gln
|
|
NM_000709.3:c.829G>C
|
NP_000700.1:p.Glu277Gln
|
|
NM_001164783.1:c.829G>C
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NP_001158255.1:p.Glu277Gln
|
|
NM_000709.4:c.829G>C
MANE Select
|
NP_000700.1:p.Glu277Gln
|
|
NM_001164783.2:c.829G>C
|
NP_001158255.1:p.Glu277Gln
|
|