ENST00000295897.9:c.1792A>T
MANE Select
|
ENSP00000295897.4:p.Lys598Ter
|
|
ENST00000295897.8:c.1792A>T
|
ENSP00000295897.4:p.Lys598Ter
|
|
ENST00000401494.7:c.1447A>T
|
ENSP00000384695.3:p.Lys483Ter
|
|
ENST00000415165.6:c.1216A>T
|
ENSP00000401820.2:p.Lys406Ter
|
|
ENST00000476441.6:c.*1071A>T
|
ENSP00000423727.1:n.*1071A>T
|
|
ENST00000495173.1:n.100A>T
|
|
|
ENST00000503124.5:c.1342A>T
|
ENSP00000421027.1:p.Lys448Ter
|
|
ENST00000505649.5:n.1339A>T
|
|
|
ENST00000508932.5:n.182A>T
|
|
|
ENST00000509063.5:c.1785+621A>T
|
ENSP00000422784.1:n.1785+621A>T
|
|
ENST00000511370.1:c.1325A>T
|
|
|
ENST00000621085.4:c.1153A>T
|
ENSP00000483421.1:p.Lys385Ter
|
|
ENST00000621628.4:c.1153A>T
|
ENSP00000480485.1:p.Lys385Ter
|
|
NM_000477.5:c.1792A>T
|
NP_000468.1:p.Lys598Ter
|
|
NM_000477.6:c.1792A>T
|
NP_000468.1:p.Lys598Ter
|
|
NM_000477.7:c.1792A>T
MANE Select
|
NP_000468.1:p.Lys598Ter
|
|