ENST00000682422.1:n.815A>G
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|
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ENST00000682545.1:c.*240A>G
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ENSP00000508402.1:n.*240A>G
|
|
ENST00000682887.1:c.1635A>G
|
ENSP00000506946.1:n.1635A>G
|
|
ENST00000683302.1:c.1165A>G
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ENSP00000507885.1:p.Thr389Ala
|
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ENST00000683557.1:c.*66A>G
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ENSP00000508029.1:n.*66A>G
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|
ENST00000367282.6:c.1234A>G
MANE Select
|
ENSP00000356251.4:p.Thr412Ala
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|
ENST00000367282.5:c.1234A>G
|
ENSP00000356251.4:p.Thr412Ala
|
|
NM_004767.3:c.1234A>G
|
NP_004758.3:p.Thr412Ala
|
|
XM_011510158.1:c.673A>G
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XP_011508460.1:p.Thr225Ala
|
|
NM_004767.4:c.1234A>G
|
NP_004758.3:p.Thr412Ala
|
|
XM_011510158.2:c.673A>G
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XP_011508460.1:p.Thr225Ala
|
|
NM_004767.5:c.1234A>G
MANE Select
|
NP_004758.3:p.Thr412Ala
|
|