ENST00000452035.7:n.2293A>T
|
|
|
ENST00000483004.2:c.1590A>T
|
ENSP00000419887.2:p.Gly530=
|
|
ENST00000698628.1:c.1625-249A>T
|
ENSP00000513848.1:n.1625-249A>T
|
|
ENST00000698629.1:n.2078A>T
|
|
|
ENST00000698630.1:n.2522A>T
|
|
|
ENST00000698631.1:n.2523A>T
|
|
|
ENST00000698632.1:n.3412A>T
|
|
|
ENST00000698633.1:n.3302A>T
|
|
|
ENST00000425368.7:c.1806A>T
MANE Select
|
ENSP00000416561.2:p.Gly602=
|
|
ENST00000425368.6:c.1806A>T
|
ENSP00000416561.2:p.Gly602=
|
|
ENST00000456570.5:c.3312A>T
|
ENSP00000410815.1:p.Gly1104=
|
|
ENST00000467360.1:n.932A>T
|
|
|
ENST00000477310.1:c.2859A>T
|
ENSP00000418996.1:p.Gly953=
|
|
ENST00000482312.1:n.22A>T
|
|
|
ENST00000483004.1:c.428A>T
|
|
|
NM_001710.5:c.1806A>T , LRG_136t1:c.1806A>T
|
NP_001701.2:p.Gly602=
|
|
NM_001710.6:c.1806A>T
MANE Select
|
NP_001701.2:p.Gly602=
|
|