ENST00000452035.7:n.2134A>T
|
|
|
ENST00000483004.2:c.1526A>T
|
ENSP00000419887.2:p.Lys509Met
|
|
ENST00000698628.1:c.1624+333A>T
|
ENSP00000513848.1:n.1624+333A>T
|
|
ENST00000698629.1:n.1919A>T
|
|
|
ENST00000698630.1:n.2458A>T
|
|
|
ENST00000698631.1:n.2459A>T
|
|
|
ENST00000698632.1:n.3253A>T
|
|
|
ENST00000698633.1:n.3143A>T
|
|
|
ENST00000698636.1:n.1964A>T
|
|
|
ENST00000425368.7:c.1742A>T
MANE Select
|
ENSP00000416561.2:p.Lys581Met
|
|
ENST00000425368.6:c.1742A>T
|
ENSP00000416561.2:p.Lys581Met
|
|
ENST00000456570.5:c.3248A>T
|
ENSP00000410815.1:p.Lys1083Met
|
|
ENST00000467360.1:n.868A>T
|
|
|
ENST00000477310.1:c.2795A>T
|
ENSP00000418996.1:p.Lys932Met
|
|
ENST00000483004.1:c.364A>T
|
|
|
NM_001710.5:c.1742A>T , LRG_136t1:c.1742A>T
|
NP_001701.2:p.Lys581Met
|
|
NM_001710.6:c.1742A>T
MANE Select
|
NP_001701.2:p.Lys581Met
|
|