ENST00000269980.7:c.776C>A
MANE Select
|
ENSP00000269980.2:p.Pro259His
|
|
ENST00000269980.6:c.776C>A
|
ENSP00000269980.2:p.Pro259His
|
|
ENST00000457836.6:c.710C>A
|
ENSP00000416000.2:p.Pro237His
|
|
ENST00000535632.5:n.405C>A
|
|
|
ENST00000540732.3:c.878C>A
|
ENSP00000443246.1:p.Pro293His
|
|
ENST00000542943.5:c.689C>A
|
ENSP00000440345.1:p.Pro230His
|
|
ENST00000545787.1:n.404C>A
|
|
|
ENST00000595085.5:c.776C>A
|
ENSP00000471150.2:p.Pro259His
|
|
NM_000709.3:c.776C>A
|
NP_000700.1:p.Pro259His
|
|
NM_001164783.1:c.776C>A
|
NP_001158255.1:p.Pro259His
|
|
NM_000709.4:c.776C>A
MANE Select
|
NP_000700.1:p.Pro259His
|
|
NM_001164783.2:c.776C>A
|
NP_001158255.1:p.Pro259His
|
|