ENST00000295897.9:c.1791A>T
MANE Select
|
ENSP00000295897.4:p.Lys597Asn
|
|
ENST00000295897.8:c.1791A>T
|
ENSP00000295897.4:p.Lys597Asn
|
|
ENST00000401494.7:c.1446A>T
|
ENSP00000384695.3:p.Lys482Asn
|
|
ENST00000415165.6:c.1215A>T
|
ENSP00000401820.2:p.Lys405Asn
|
|
ENST00000476441.6:c.*1070A>T
|
ENSP00000423727.1:n.*1070A>T
|
|
ENST00000495173.1:n.99A>T
|
|
|
ENST00000503124.5:c.1341A>T
|
ENSP00000421027.1:p.Lys447Asn
|
|
ENST00000505649.5:n.1338A>T
|
|
|
ENST00000508932.5:n.181A>T
|
|
|
ENST00000509063.5:c.1785+620A>T
|
ENSP00000422784.1:n.1785+620A>T
|
|
ENST00000511370.1:c.1324A>T
|
|
|
ENST00000621085.4:c.1152A>T
|
ENSP00000483421.1:p.Lys384Asn
|
|
ENST00000621628.4:c.1152A>T
|
ENSP00000480485.1:p.Lys384Asn
|
|
NM_000477.5:c.1791A>T
|
NP_000468.1:p.Lys597Asn
|
|
NM_000477.6:c.1791A>T
|
NP_000468.1:p.Lys597Asn
|
|
NM_000477.7:c.1791A>T
MANE Select
|
NP_000468.1:p.Lys597Asn
|
|