ENST00000269980.7:c.1016G>T
MANE Select
|
ENSP00000269980.2:p.Ser339Ile
|
|
ENST00000269980.6:c.1016G>T
|
ENSP00000269980.2:p.Ser339Ile
|
|
ENST00000457836.6:c.1025G>T
|
ENSP00000416000.2:p.Ser342Ile
|
|
ENST00000540732.3:c.1118G>T
|
ENSP00000443246.1:p.Ser373Ile
|
|
ENST00000542943.5:c.929G>T
|
ENSP00000440345.1:p.Ser310Ile
|
|
ENST00000595085.5:c.922+321G>T
|
ENSP00000471150.2:n.922+321G>T
|
|
NM_000709.3:c.1016G>T
|
NP_000700.1:p.Ser339Ile
|
|
NM_001164783.1:c.1013G>T
|
NP_001158255.1:p.Ser338Ile
|
|
NM_000709.4:c.1016G>T
MANE Select
|
NP_000700.1:p.Ser339Ile
|
|
NM_001164783.2:c.1013G>T
|
NP_001158255.1:p.Ser338Ile
|
|