ENST00000578493.2:n.765A>G
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ENST00000699291.1:c.557A>G
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ENSP00000514272.1:p.His186Arg
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ENST00000699292.1:n.472A>G
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ENST00000225275.4:c.1432A>G
MANE Select
|
ENSP00000225275.3:p.Thr478Ala
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ENST00000225275.3:c.1432A>G
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ENSP00000225275.3:p.Thr478Ala
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NM_000250.1:c.1432A>G , LRG_84t1:c.1432A>G
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NP_000241.1:p.Thr478Ala
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XM_011524821.1:c.1618A>G
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XP_011523123.1:p.Thr540Ala
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XM_011524822.1:c.1147A>G
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XP_011523124.1:p.Thr383Ala
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XM_011524823.1:c.1457A>G
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XP_011523125.1:p.His486Arg
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NM_000250.2:c.1432A>G
MANE Select
|
NP_000241.1:p.Thr478Ala
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