ENST00000269980.7:c.692T>A
MANE Select
|
ENSP00000269980.2:p.Val231Asp
|
|
ENST00000269980.6:c.692T>A
|
ENSP00000269980.2:p.Val231Asp
|
|
ENST00000457836.6:c.626T>A
|
ENSP00000416000.2:p.Val209Asp
|
|
ENST00000535632.5:n.321T>A
|
|
|
ENST00000540732.3:c.794T>A
|
ENSP00000443246.1:p.Val265Asp
|
|
ENST00000541315.1:c.592T>A
|
|
|
ENST00000542943.5:c.605T>A
|
ENSP00000440345.1:p.Val202Asp
|
|
ENST00000545787.1:n.320T>A
|
|
|
ENST00000595085.5:c.692T>A
|
ENSP00000471150.2:p.Val231Asp
|
|
NM_000709.3:c.692T>A
|
NP_000700.1:p.Val231Asp
|
|
NM_001164783.1:c.692T>A
|
NP_001158255.1:p.Val231Asp
|
|
NM_000709.4:c.692T>A
MANE Select
|
NP_000700.1:p.Val231Asp
|
|
NM_001164783.2:c.692T>A
|
NP_001158255.1:p.Val231Asp
|
|