ENST00000696142.1:c.*254A>T
|
ENSP00000512434.1:n.*254A>T
|
|
ENST00000696143.1:c.713A>T
|
ENSP00000512435.1:n.713A>T
|
|
ENST00000696153.1:c.688A>T
|
ENSP00000512444.1:p.Asn230Tyr
|
|
ENST00000256474.3:c.577A>T
MANE Select
|
ENSP00000256474.3:p.Asn193Tyr
|
|
ENST00000256474.2:c.577A>T
|
ENSP00000256474.2:p.Asn193Tyr
|
|
ENST00000345392.2:c.454A>T
|
ENSP00000344757.2:p.Asn152Tyr
|
|
ENST00000477538.1:n.713A>T
|
|
|
NM_000551.3:c.577A>T , LRG_322t1:c.577A>T
|
NP_000542.1:p.Asn193Tyr
|
|
NM_198156.2:c.454A>T
|
NP_937799.1:p.Asn152Tyr
|
|
NM_001354723.1:c.*131A>T
|
NP_001341652.1:n.*131A>T
|
|
NM_000551.4:c.577A>T
MANE Select
|
NP_000542.1:p.Asn193Tyr
|
|
NM_001354723.2:c.*131A>T
|
NP_001341652.1:n.*131A>T
|
|
NM_198156.3:c.454A>T
|
NP_937799.1:p.Asn152Tyr
|
|