ENST00000281928.9:c.5163T>G
MANE Select
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ENSP00000281928.3:p.Ser1721=
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ENST00000549786.2:c.4591T>G
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|
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ENST00000648379.1:n.3531T>G
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ENST00000648737.1:n.4927T>G
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|
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ENST00000648825.1:n.1903T>G
|
|
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ENST00000648916.1:n.3174T>G
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|
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ENST00000649146.1:n.2406T>G
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|
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ENST00000649607.1:c.3347T>G
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|
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ENST00000649775.1:c.1652T>G
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|
|
ENST00000650226.1:c.5163T>G
|
ENSP00000496981.1:p.Ser1721=
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ENST00000281928.7:c.5163T>G
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ENSP00000281928.3:p.Ser1721=
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ENST00000549786.1:c.527T>G
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|
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ENST00000552340.1:c.195T>G
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ENSP00000449876.1:p.Ser65=
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|
NM_015335.4:c.5163T>G
|
NP_056150.1:p.Ser1721=
|
|
XM_011538080.1:c.5163T>G
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XP_011536382.1:p.Ser1721=
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XM_011538081.1:c.5160T>G
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XP_011536383.1:p.Ser1720=
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XM_011538082.1:c.5133T>G
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XP_011536384.1:p.Ser1711=
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XM_011538080.2:c.5163T>G
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XP_011536382.1:p.Ser1721=
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|
XM_011538081.2:c.5160T>G
|
XP_011536383.1:p.Ser1720=
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|
XM_011538082.2:c.5133T>G
|
XP_011536384.1:p.Ser1711=
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|
XM_017019090.1:c.5160T>G
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XP_016874579.1:p.Ser1720=
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NM_015335.5:c.5163T>G
MANE Select
|
NP_056150.1:p.Ser1721=
|
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