ENST00000452035.7:n.210G>T
|
|
|
ENST00000483004.2:c.33G>T
|
ENSP00000419887.2:p.Leu11=
|
|
ENST00000497841.6:c.33G>T
|
ENSP00000513847.1:p.Leu11=
|
|
ENST00000698628.1:c.33G>T
|
ENSP00000513848.1:p.Leu11=
|
|
ENST00000698629.1:n.210G>T
|
|
|
ENST00000698630.1:n.194G>T
|
|
|
ENST00000698631.1:n.189G>T
|
|
|
ENST00000698632.1:n.161G>T
|
|
|
ENST00000698633.1:n.131G>T
|
|
|
ENST00000698636.1:n.255G>T
|
|
|
ENST00000425368.7:c.33G>T
MANE Select
|
ENSP00000416561.2:p.Leu11=
|
|
ENST00000425368.6:c.33G>T
|
ENSP00000416561.2:p.Leu11=
|
|
ENST00000452035.6:n.33G>T
|
|
|
ENST00000456570.5:c.1571-119G>T
|
ENSP00000410815.1:n.1571-119G>T
|
|
ENST00000460718.5:c.33G>T
|
ENSP00000417793.1:p.Leu11=
|
|
ENST00000472581.1:n.280G>T
|
|
|
ENST00000475617.5:c.33G>T
|
ENSP00000420090.1:p.Leu11=
|
|
ENST00000477310.1:c.1352-753G>T
|
ENSP00000418996.1:n.1352-753G>T
|
|
NM_001710.5:c.33G>T , LRG_136t1:c.33G>T
|
NP_001701.2:p.Leu11=
|
|
NM_001710.6:c.33G>T
MANE Select
|
NP_001701.2:p.Leu11=
|
|