ENST00000452035.7:n.2018A>C
|
|
|
ENST00000483004.2:c.1410A>C
|
ENSP00000419887.2:p.Gly470=
|
|
ENST00000698628.1:c.1624+217A>C
|
ENSP00000513848.1:n.1624+217A>C
|
|
ENST00000698629.1:n.1803A>C
|
|
|
ENST00000698630.1:n.2342A>C
|
|
|
ENST00000698631.1:n.2343A>C
|
|
|
ENST00000698632.1:n.3137A>C
|
|
|
ENST00000698633.1:n.3027A>C
|
|
|
ENST00000698636.1:n.1848A>C
|
|
|
ENST00000425368.7:c.1626A>C
MANE Select
|
ENSP00000416561.2:p.Gly542=
|
|
ENST00000425368.6:c.1626A>C
|
ENSP00000416561.2:p.Gly542=
|
|
ENST00000452035.6:n.1841A>C
|
|
|
ENST00000456570.5:c.3132A>C
|
ENSP00000410815.1:p.Gly1044=
|
|
ENST00000467360.1:n.752A>C
|
|
|
ENST00000477310.1:c.2679A>C
|
ENSP00000418996.1:p.Gly893=
|
|
ENST00000483004.1:c.248A>C
|
|
|
NM_001710.5:c.1626A>C , LRG_136t1:c.1626A>C
|
NP_001701.2:p.Gly542=
|
|
NM_001710.6:c.1626A>C
MANE Select
|
NP_001701.2:p.Gly542=
|
|