ENST00000696142.1:c.*146A>G
|
ENSP00000512434.1:n.*146A>G
|
|
ENST00000696143.1:c.605A>G
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ENSP00000512435.1:n.605A>G
|
|
ENST00000696153.1:c.580A>G
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ENSP00000512444.1:p.Thr194Ala
|
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ENST00000256474.3:c.469A>G
MANE Select
|
ENSP00000256474.3:p.Thr157Ala
|
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ENST00000256474.2:c.469A>G
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ENSP00000256474.2:p.Thr157Ala
|
|
ENST00000345392.2:c.346A>G
|
ENSP00000344757.2:p.Thr116Ala
|
|
ENST00000477538.1:n.605A>G
|
|
|
NM_000551.3:c.469A>G , LRG_322t1:c.469A>G
|
NP_000542.1:p.Thr157Ala
|
|
NM_198156.2:c.346A>G
|
NP_937799.1:p.Thr116Ala
|
|
NM_001354723.1:c.*23A>G
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NP_001341652.1:n.*23A>G
|
|
NM_000551.4:c.469A>G
MANE Select
|
NP_000542.1:p.Thr157Ala
|
|
NM_001354723.2:c.*23A>G
|
NP_001341652.1:n.*23A>G
|
|
NM_198156.3:c.346A>G
|
NP_937799.1:p.Thr116Ala
|
|