ENST00000389048.8:c.3556A>G
MANE Select
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ENSP00000373700.3:p.Ser1186Gly
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ENST00000431873.6:c.783A>G
|
|
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ENST00000638605.1:n.433A>G
|
|
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ENST00000642122.1:c.352A>G
|
ENSP00000493203.1:p.Ser118Gly
|
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ENST00000389048.7:c.3556A>G
|
ENSP00000373700.3:p.Ser1186Gly
|
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ENST00000431873.5:c.436A>G
|
ENSP00000414027.2:p.Ser146Gly
|
|
ENST00000618119.4:c.2425A>G
|
ENSP00000482733.1:p.Ser809Gly
|
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NM_004304.4:c.3556A>G
|
NP_004295.2:p.Ser1186Gly
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NM_001353765.1:c.352A>G
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NP_001340694.1:p.Ser118Gly
|
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XM_024452778.1:c.709A>G
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XP_024308546.1:p.Ser237Gly
|
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XM_024452779.1:c.352A>G
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XP_024308547.1:p.Ser118Gly
|
|
NM_004304.5:c.3556A>G
MANE Select
|
NP_004295.2:p.Ser1186Gly
|
|
NM_001353765.2:c.352A>G
|
NP_001340694.1:p.Ser118Gly
|
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