ENST00000281928.9:c.5077T>G
MANE Select
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ENSP00000281928.3:p.Ser1693Ala
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ENST00000549786.2:c.4505T>G
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|
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ENST00000648379.1:n.3445T>G
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|
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ENST00000648737.1:n.4841T>G
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|
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ENST00000648825.1:n.1817T>G
|
|
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ENST00000648916.1:n.3088T>G
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|
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ENST00000649146.1:n.2320T>G
|
|
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ENST00000649607.1:c.3261T>G
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|
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ENST00000649775.1:c.1566T>G
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|
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ENST00000650226.1:c.5077T>G
|
ENSP00000496981.1:p.Ser1693Ala
|
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ENST00000281928.7:c.5077T>G
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ENSP00000281928.3:p.Ser1693Ala
|
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ENST00000549786.1:c.441T>G
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|
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ENST00000552340.1:c.109T>G
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ENSP00000449876.1:p.Ser37Ala
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NM_015335.4:c.5077T>G
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NP_056150.1:p.Ser1693Ala
|
|
XM_011538080.1:c.5077T>G
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XP_011536382.1:p.Ser1693Ala
|
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XM_011538081.1:c.5074T>G
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XP_011536383.1:p.Ser1692Ala
|
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XM_011538082.1:c.5047T>G
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XP_011536384.1:p.Ser1683Ala
|
|
XM_011538080.2:c.5077T>G
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XP_011536382.1:p.Ser1693Ala
|
|
XM_011538081.2:c.5074T>G
|
XP_011536383.1:p.Ser1692Ala
|
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XM_011538082.2:c.5047T>G
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XP_011536384.1:p.Ser1683Ala
|
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XM_017019090.1:c.5074T>G
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XP_016874579.1:p.Ser1692Ala
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NM_015335.5:c.5077T>G
MANE Select
|
NP_056150.1:p.Ser1693Ala
|
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