ENST00000369689.6:c.261A>G
MANE Select
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ENSP00000358703.1:p.Lys87=
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ENST00000369687.2:c.87A>G
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ENSP00000358701.1:p.Lys29=
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ENST00000369689.5:c.261A>G
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ENSP00000358703.1:p.Lys87=
|
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ENST00000635617.1:n.3674A>G
|
|
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NM_001009994.2:c.261A>G
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NP_001009994.1:p.Lys87=
|
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NR_103525.1:n.318A>G
|
|
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NR_103525.2:n.256A>G
|
|
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NM_001009994.3:c.261A>G
MANE Select
|
NP_001009994.1:p.Lys87=
|
|
NM_001400774.1:c.-28+3102A>G
|
NP_001387703.1:n.-28+3102A>G
|
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NM_001400899.1:c.324A>G
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NP_001387828.1:p.Lys108=
|
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NM_001400900.1:c.*3098A>G
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NP_001387829.1:n.*3098A>G
|
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NR_174603.1:n.234+3102A>G
|
|
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NR_174604.1:n.296+3102A>G
|
|
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NR_174605.1:n.455+3204A>G
|
|
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NR_174622.1:n.3336A>G
|
|
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