ENST00000452035.7:n.2071A>C
|
|
|
ENST00000483004.2:c.1463A>C
|
ENSP00000419887.2:p.Asn488Thr
|
|
ENST00000698628.1:c.1624+270A>C
|
ENSP00000513848.1:n.1624+270A>C
|
|
ENST00000698629.1:n.1856A>C
|
|
|
ENST00000698630.1:n.2395A>C
|
|
|
ENST00000698631.1:n.2396A>C
|
|
|
ENST00000698632.1:n.3190A>C
|
|
|
ENST00000698633.1:n.3080A>C
|
|
|
ENST00000698636.1:n.1901A>C
|
|
|
ENST00000425368.7:c.1679A>C
MANE Select
|
ENSP00000416561.2:p.Asn560Thr
|
|
ENST00000425368.6:c.1679A>C
|
ENSP00000416561.2:p.Asn560Thr
|
|
ENST00000456570.5:c.3185A>C
|
ENSP00000410815.1:p.Asn1062Thr
|
|
ENST00000467360.1:n.805A>C
|
|
|
ENST00000477310.1:c.2732A>C
|
ENSP00000418996.1:p.Asn911Thr
|
|
ENST00000483004.1:c.301A>C
|
|
|
NM_001710.5:c.1679A>C , LRG_136t1:c.1679A>C
|
NP_001701.2:p.Asn560Thr
|
|
NM_001710.6:c.1679A>C
MANE Select
|
NP_001701.2:p.Asn560Thr
|
|