ENST00000295897.9:c.1789A>T
MANE Select
|
ENSP00000295897.4:p.Lys597Ter
|
|
ENST00000295897.8:c.1789A>T
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ENSP00000295897.4:p.Lys597Ter
|
|
ENST00000401494.7:c.1444A>T
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ENSP00000384695.3:p.Lys482Ter
|
|
ENST00000415165.6:c.1213A>T
|
ENSP00000401820.2:p.Lys405Ter
|
|
ENST00000476441.6:c.*1068A>T
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ENSP00000423727.1:n.*1068A>T
|
|
ENST00000495173.1:n.97A>T
|
|
|
ENST00000503124.5:c.1339A>T
|
ENSP00000421027.1:p.Lys447Ter
|
|
ENST00000505649.5:n.1336A>T
|
|
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ENST00000508932.5:n.179A>T
|
|
|
ENST00000509063.5:c.1785+618A>T
|
ENSP00000422784.1:n.1785+618A>T
|
|
ENST00000511370.1:c.1322A>T
|
|
|
ENST00000621085.4:c.1150A>T
|
ENSP00000483421.1:p.Lys384Ter
|
|
ENST00000621628.4:c.1150A>T
|
ENSP00000480485.1:p.Lys384Ter
|
|
NM_000477.5:c.1789A>T
|
NP_000468.1:p.Lys597Ter
|
|
NM_000477.6:c.1789A>T
|
NP_000468.1:p.Lys597Ter
|
|
NM_000477.7:c.1789A>T
MANE Select
|
NP_000468.1:p.Lys597Ter
|
|