ENST00000452035.7:n.2549T>G
|
|
|
ENST00000483004.2:c.1899T>G
|
ENSP00000419887.2:p.Val633=
|
|
ENST00000698628.1:c.1884T>G
|
ENSP00000513848.1:p.Val628=
|
|
ENST00000698629.1:n.2334T>G
|
|
|
ENST00000698630.1:n.2831T>G
|
|
|
ENST00000698631.1:n.2832T>G
|
|
|
ENST00000698632.1:n.3920T>G
|
|
|
ENST00000698633.1:n.3810T>G
|
|
|
ENST00000425368.7:c.2115T>G
MANE Select
|
ENSP00000416561.2:p.Val705=
|
|
ENST00000425368.6:c.2115T>G
|
ENSP00000416561.2:p.Val705=
|
|
ENST00000456570.5:c.3621T>G
|
ENSP00000410815.1:p.Val1207=
|
|
ENST00000477310.1:c.3168T>G
|
ENSP00000418996.1:p.Val1056=
|
|
ENST00000482312.1:n.530T>G
|
|
|
ENST00000483004.1:c.737T>G
|
|
|
ENST00000498317.1:c.85T>G
|
|
|
NM_001710.5:c.2115T>G , LRG_136t1:c.2115T>G
|
NP_001701.2:p.Val705=
|
|
NM_001710.6:c.2115T>G
MANE Select
|
NP_001701.2:p.Val705=
|
|