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NM_017652.4:c.10G>T
MANE Select
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NP_060122.2:p.Ala4Ser
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ENST00000396154.7:c.10G>T
MANE Select
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ENSP00000379458.1:p.Ala4Ser
|
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NM_001077426.2:c.10G>T
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NP_001070894.1:p.Ala4Ser
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NM_001077426.3:c.10G>T
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NP_001070894.1:p.Ala4Ser
|
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NM_001204814.1:c.-170G>T
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NP_001191743.1:n.-170G>T
|
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NM_001204814.2:c.-170G>T
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NP_001191743.1:n.-170G>T
|
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NM_017652.3:c.10G>T
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NP_060122.2:p.Ala4Ser
|
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ENST00000391702.3:c.-170G>T
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ENSP00000375583.3:n.-170G>T
|
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ENST00000396150.4:c.10G>T
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ENSP00000379454.3:p.Ala4Ser
|
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ENST00000396154.6:c.10G>T
|
ENSP00000379458.1:p.Ala4Ser
|
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ENST00000598183.1:c.10G>T
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ENSP00000471663.1:p.Ala4Ser
|
|
ENST00000598885.5:c.10G>T
|
ENSP00000470397.1:p.Ala4Ser
|
|
ENST00000599802.1:c.10G>T
|
ENSP00000472972.1:p.Ala4Ser
|
|
ENST00000651718.1:c.10G>T
|
ENSP00000498256.1:p.Ala4Ser
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