ENST00000452035.7:n.2143A>C
|
|
|
ENST00000483004.2:c.1535A>C
|
ENSP00000419887.2:p.Asn512Thr
|
|
ENST00000698628.1:c.1624+342A>C
|
ENSP00000513848.1:n.1624+342A>C
|
|
ENST00000698629.1:n.1928A>C
|
|
|
ENST00000698630.1:n.2467A>C
|
|
|
ENST00000698631.1:n.2468A>C
|
|
|
ENST00000698632.1:n.3262A>C
|
|
|
ENST00000698633.1:n.3152A>C
|
|
|
ENST00000698636.1:n.1973A>C
|
|
|
ENST00000425368.7:c.1751A>C
MANE Select
|
ENSP00000416561.2:p.Asn584Thr
|
|
ENST00000425368.6:c.1751A>C
|
ENSP00000416561.2:p.Asn584Thr
|
|
ENST00000456570.5:c.3257A>C
|
ENSP00000410815.1:p.Asn1086Thr
|
|
ENST00000467360.1:n.877A>C
|
|
|
ENST00000477310.1:c.2804A>C
|
ENSP00000418996.1:p.Asn935Thr
|
|
ENST00000483004.1:c.373A>C
|
|
|
NM_001710.5:c.1751A>C , LRG_136t1:c.1751A>C
|
NP_001701.2:p.Asn584Thr
|
|
NM_001710.6:c.1751A>C
MANE Select
|
NP_001701.2:p.Asn584Thr
|
|