ENST00000357578.8:c.1288C>T
MANE Select
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ENSP00000350191.3:p.Gln430Ter
|
|
ENST00000479394.2:n.403C>T
|
|
|
ENST00000672352.1:c.907C>T
|
ENSP00000500876.1:p.Gln303Ter
|
|
ENST00000672652.1:c.1251C>T
|
|
|
ENST00000348925.2:c.1327C>T
|
ENSP00000314649.3:p.Gln443Ter
|
|
ENST00000357578.7:c.1288C>T
|
ENSP00000350191.3:p.Gln430Ter
|
|
ENST00000479394.1:n.403C>T
|
|
|
ENST00000491546.5:c.1204C>T
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ENSP00000417687.1:p.Gln402Ter
|
|
NM_001080.3:c.1288C>T
MANE Select
|
NP_001071.1:p.Gln430Ter
|
|
NM_170740.1:c.1327C>T
|
NP_733936.1:p.Gln443Ter
|
|
NM_001368954.1:c.1144C>T
|
NP_001355883.1:p.Gln382Ter
|
|