ENST00000269980.7:c.1014C>A
MANE Select
|
ENSP00000269980.2:p.Thr338=
|
|
ENST00000269980.6:c.1014C>A
|
ENSP00000269980.2:p.Thr338=
|
|
ENST00000457836.6:c.1023C>A
|
ENSP00000416000.2:p.Thr341=
|
|
ENST00000540732.3:c.1116C>A
|
ENSP00000443246.1:p.Thr372=
|
|
ENST00000542943.5:c.927C>A
|
ENSP00000440345.1:p.Thr309=
|
|
ENST00000595085.5:c.922+319C>A
|
ENSP00000471150.2:n.922+319C>A
|
|
NM_000709.3:c.1014C>A
|
NP_000700.1:p.Thr338=
|
|
NM_001164783.1:c.1011C>A
|
NP_001158255.1:p.Thr337=
|
|
NM_000709.4:c.1014C>A
MANE Select
|
NP_000700.1:p.Thr338=
|
|
NM_001164783.2:c.1011C>A
|
NP_001158255.1:p.Thr337=
|
|