ENST00000394867.9:n.1181T>G
|
|
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ENST00000687128.1:n.1181T>G
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|
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ENST00000688002.1:n.1036T>G
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|
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ENST00000689792.1:n.646T>G
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|
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ENST00000262948.10:c.742T>G
MANE Select
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ENSP00000262948.4:p.Ser248Ala
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ENST00000262948.9:c.742T>G
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ENSP00000262948.3:p.Ser248Ala
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ENST00000394867.8:c.451T>G
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ENSP00000378336.1:p.Ser151Ala
|
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ENST00000593364.5:n.689T>G
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|
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ENST00000595715.1:n.557T>G
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|
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ENST00000597263.5:n.169+1641T>G
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|
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ENST00000599021.1:c.29+1641T>G
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|
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ENST00000600584.5:n.1302T>G
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|
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ENST00000601786.5:n.1043T>G
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|
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NM_030662.3:c.742T>G , LRG_750t1:c.742T>G
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NP_109587.1:p.Ser248Ala
|
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XM_006722799.2:c.705+1641T>G
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XP_006722862.1:n.705+1641T>G
|
|
XM_011528133.1:c.172T>G
|
XP_011526435.1:p.Ser58Ala
|
|
XM_017026989.1:c.742T>G
|
XP_016882478.1:p.Ser248Ala
|
|
XM_017026990.1:c.705+1641T>G
|
XP_016882479.1:n.705+1641T>G
|
|
NM_030662.4:c.742T>G
MANE Select
|
NP_109587.1:p.Ser248Ala
|
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