ENST00000369689.6:c.293C>T
MANE Select
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ENSP00000358703.1:p.Ala98Val
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ENST00000369687.2:c.119C>T
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ENSP00000358701.1:p.Ala40Val
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ENST00000369689.5:c.293C>T
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ENSP00000358703.1:p.Ala98Val
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ENST00000635617.1:n.3706C>T
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NM_001009994.2:c.293C>T
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NP_001009994.1:p.Ala98Val
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NR_103525.1:n.350C>T
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NR_103525.2:n.288C>T
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NM_001009994.3:c.293C>T
MANE Select
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NP_001009994.1:p.Ala98Val
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NM_001400774.1:c.-28+3134C>T
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NP_001387703.1:n.-28+3134C>T
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NM_001400899.1:c.356C>T
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NP_001387828.1:p.Ala119Val
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NM_001400900.1:c.*3130C>T
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NP_001387829.1:n.*3130C>T
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NR_174603.1:n.234+3134C>T
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NR_174604.1:n.296+3134C>T
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NR_174605.1:n.455+3236C>T
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NR_174622.1:n.3368C>T
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