ENST00000269980.7:c.1335G>A
MANE Select
|
ENSP00000269980.2:p.Lys445=
|
|
ENST00000269980.6:c.1335G>A
|
ENSP00000269980.2:p.Lys445=
|
|
ENST00000457836.6:c.1344G>A
|
ENSP00000416000.2:p.Lys448=
|
|
ENST00000540732.3:c.1437G>A
|
ENSP00000443246.1:p.Lys479=
|
|
ENST00000544905.1:c.165G>A
|
|
|
ENST00000595085.5:c.922+1908G>A
|
ENSP00000471150.2:n.922+1908G>A
|
|
NM_000709.3:c.1335G>A
|
NP_000700.1:p.Lys445=
|
|
NM_001164783.1:c.1332G>A
|
NP_001158255.1:p.Lys444=
|
|
NM_000709.4:c.1335G>A
MANE Select
|
NP_000700.1:p.Lys445=
|
|
NM_001164783.2:c.1332G>A
|
NP_001158255.1:p.Lys444=
|
|