ENST00000692008.1:c.216G=
MANE Select
|
ENSP00000509398.1:p.Leu72=
|
|
ENST00000293308.11:c.216G=
|
ENSP00000293308.6:p.Leu72=
|
|
ENST00000546542.1:c.450G=
|
ENSP00000450228.1:p.Leu150=
|
|
ENST00000546583.5:n.287G=
|
|
|
ENST00000546826.5:c.216G=
|
ENSP00000447881.1:p.Leu72=
|
|
ENST00000546897.5:c.216G=
|
ENSP00000447402.1:p.Leu72=
|
|
ENST00000548998.5:c.336G=
|
ENSP00000447040.1:p.Leu112=
|
|
ENST00000550170.5:n.279G=
|
|
|
ENST00000552150.5:c.300G=
|
ENSP00000449404.1:p.Leu100=
|
|
ENST00000552551.5:c.216G=
|
ENSP00000447566.1:p.Leu72=
|
|
NM_001256282.1:c.300G=
|
NP_001243211.1:p.Leu100=
|
|
NM_001256293.1:c.216G=
|
NP_001243222.1:p.Leu72=
|
|
NM_002273.3:c.216G=
|
NP_002264.1:p.Leu72=
|
|
NR_045962.1:n.673G=
|
|
|
NM_001256282.2:c.300G=
|
NP_001243211.1:p.Leu100=
|
|
NM_001256293.2:c.216G=
|
NP_001243222.1:p.Leu72=
|
|
NM_002273.4:c.216G=
MANE Select
|
NP_002264.1:p.Leu72=
|
|
NR_045962.2:n.667G=
|
|
|