ENST00000254108.12:c.905C>T
MANE Select
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ENSP00000254108.8:p.Ala302Val
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ENST00000254108.11:c.905C>T
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ENSP00000254108.7:p.Ala302Val
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ENST00000380244.7:c.902C>T
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ENSP00000369594.3:p.Ala301Val
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ENST00000474990.5:n.199C>T
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ENST00000487509.6:n.4080C>T
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ENST00000564766.1:n.729C>T
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ENST00000566605.5:c.*78C>T
|
ENSP00000455073.1:n.*78C>T
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ENST00000568685.1:c.908C>T
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ENSP00000455282.1:p.Ala303Val
|
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ENST00000568901.2:n.279C>T
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NM_001170634.1:c.902C>T
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NP_001164105.1:p.Ala301Val
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NM_001170937.1:c.893C>T
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NP_001164408.1:p.Ala298Val
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NM_004960.3:c.905C>T , LRG_655t1:c.905C>T
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NP_004951.1:p.Ala302Val
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NR_028388.2:n.975C>T
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XM_005255233.3:c.290C>T
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XP_005255290.1:p.Ala97Val
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XM_011545781.1:c.899C>T
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XP_011544083.1:p.Ala300Val
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XM_011545782.1:c.290C>T
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XP_011544084.1:p.Ala97Val
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XM_005255233.5:c.290C>T
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XP_005255290.1:p.Ala97Val
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XM_011545782.2:c.290C>T
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XP_011544084.1:p.Ala97Val
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XM_024450221.1:c.896C>T
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XP_024305989.1:p.Ala299Val
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NM_004960.4:c.905C>T
MANE Select
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NP_004951.1:p.Ala302Val
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