ENST00000269980.7:c.777C>T
MANE Select
|
ENSP00000269980.2:p.Pro259=
|
|
ENST00000269980.6:c.777C>T
|
ENSP00000269980.2:p.Pro259=
|
|
ENST00000457836.6:c.711C>T
|
ENSP00000416000.2:p.Pro237=
|
|
ENST00000535632.5:n.406C>T
|
|
|
ENST00000540732.3:c.879C>T
|
ENSP00000443246.1:p.Pro293=
|
|
ENST00000542943.5:c.690C>T
|
ENSP00000440345.1:p.Pro230=
|
|
ENST00000545787.1:n.405C>T
|
|
|
ENST00000595085.5:c.777C>T
|
ENSP00000471150.2:p.Pro259=
|
|
NM_000709.3:c.777C>T
|
NP_000700.1:p.Pro259=
|
|
NM_001164783.1:c.777C>T
|
NP_001158255.1:p.Pro259=
|
|
NM_000709.4:c.777C>T
MANE Select
|
NP_000700.1:p.Pro259=
|
|
NM_001164783.2:c.777C>T
|
NP_001158255.1:p.Pro259=
|
|