ENST00000703783.1:n.931T>G
|
|
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ENST00000703785.1:n.1012T>G
|
|
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ENST00000262464.9:c.4147T>G
MANE Select
|
ENSP00000262464.4:p.Ser1383Ala
|
|
ENST00000262464.8:c.4147T>G
|
ENSP00000262464.4:p.Ser1383Ala
|
|
ENST00000507835.5:c.697T>G
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ENSP00000426839.1:p.Ser233Ala
|
|
ENST00000508053.5:c.4147T>G
|
ENSP00000424571.1:p.Ser1383Ala
|
|
ENST00000508989.5:c.4048T>G
|
ENSP00000425596.1:p.Ser1350Ala
|
|
ENST00000619499.4:c.4144T>G
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ENSP00000482132.1:p.Ser1382Ala
|
|
NM_001999.3:c.4147T>G
|
NP_001990.2:p.Ser1383Ala
|
|
XM_017009228.2:c.3994T>G
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XP_016864717.1:p.Ser1332Ala
|
|
NM_001999.4:c.4147T>G
MANE Select
|
NP_001990.2:p.Ser1383Ala
|
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