ENST00000420175.3:c.183A>T
MANE Select
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ENSP00000391137.2:p.Ala61=
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ENST00000275838.5:c.183A>T
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ENSP00000275838.1:p.Ala61=
|
|
ENST00000377867.7:c.272-289A>T
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ENSP00000367098.3:n.272-289A>T
|
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ENST00000415615.1:c.*227A>T
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ENSP00000410871.1:n.*227A>T
|
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ENST00000420175.2:c.183A>T
|
ENSP00000391137.2:p.Ala61=
|
|
NM_001142459.1:c.183A>T
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NP_001135931.2:p.Ala61=
|
|
NM_001142460.1:c.183A>T
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NP_001135932.2:p.Ala61=
|
|
NM_080871.3:c.272-289A>T
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NP_543147.2:n.272-289A>T
|
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XM_005249949.3:c.318A>T
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XP_005250006.1:p.Ala106=
|
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NM_001142459.2:c.183A>T
MANE Select
|
NP_001135931.2:p.Ala61=
|
|
NM_080871.4:c.272-289A>T
|
NP_543147.2:n.272-289A>T
|
|