ENST00000269980.7:c.742G>T
MANE Select
|
ENSP00000269980.2:p.Ala248Ser
|
|
ENST00000269980.6:c.742G>T
|
ENSP00000269980.2:p.Ala248Ser
|
|
ENST00000457836.6:c.676G>T
|
ENSP00000416000.2:p.Ala226Ser
|
|
ENST00000535632.5:n.371G>T
|
|
|
ENST00000540732.3:c.844G>T
|
ENSP00000443246.1:p.Ala282Ser
|
|
ENST00000542943.5:c.655G>T
|
ENSP00000440345.1:p.Ala219Ser
|
|
ENST00000545787.1:n.370G>T
|
|
|
ENST00000595085.5:c.742G>T
|
ENSP00000471150.2:p.Ala248Ser
|
|
NM_000709.3:c.742G>T
|
NP_000700.1:p.Ala248Ser
|
|
NM_001164783.1:c.742G>T
|
NP_001158255.1:p.Ala248Ser
|
|
NM_000709.4:c.742G>T
MANE Select
|
NP_000700.1:p.Ala248Ser
|
|
NM_001164783.2:c.742G>T
|
NP_001158255.1:p.Ala248Ser
|
|