ENST00000269980.7:c.1233C>T
MANE Select
|
ENSP00000269980.2:p.Asp411=
|
|
ENST00000269980.6:c.1233C>T
|
ENSP00000269980.2:p.Asp411=
|
|
ENST00000457836.6:c.1242C>T
|
ENSP00000416000.2:p.Asp414=
|
|
ENST00000540732.3:c.1335C>T
|
ENSP00000443246.1:p.Asp445=
|
|
ENST00000544905.1:c.63C>T
|
|
|
ENST00000595085.5:c.922+1806C>T
|
ENSP00000471150.2:n.922+1806C>T
|
|
NM_000709.3:c.1233C>T
|
NP_000700.1:p.Asp411=
|
|
NM_001164783.1:c.1230C>T
|
NP_001158255.1:p.Asp410=
|
|
NM_000709.4:c.1233C>T
MANE Select
|
NP_000700.1:p.Asp411=
|
|
NM_001164783.2:c.1230C>T
|
NP_001158255.1:p.Asp410=
|
|