ENST00000231887.8:c.4G>T
MANE Select
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ENSP00000231887.3:p.Ala2Ser
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ENST00000231887.7:c.4G>T
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ENSP00000231887.3:p.Ala2Ser
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ENST00000440662.1:c.4G>T
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ENSP00000396798.1:p.Ala2Ser
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ENST00000456310.5:c.-408G>T
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ENSP00000387746.1:n.-408G>T
|
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ENST00000465178.1:n.228-5502G>T
|
|
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ENST00000475987.1:n.31G>T
|
|
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NM_001166415.1:c.-408G>T
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NP_001159887.1:n.-408G>T
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NM_001966.3:c.4G>T
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NP_001957.2:p.Ala2Ser
|
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XM_006713525.1:c.-652G>T
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XP_006713588.1:n.-652G>T
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XM_011512517.1:c.-214-5502G>T
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XP_011510819.1:n.-214-5502G>T
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NM_001966.4:c.4G>T
MANE Select
|
NP_001957.2:p.Ala2Ser
|
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NM_001166415.2:c.-408G>T
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NP_001159887.1:n.-408G>T
|
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