ENST00000703783.1:n.550C>G
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|
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ENST00000703785.1:n.631C>G
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|
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ENST00000262464.9:c.3766C>G
MANE Select
|
ENSP00000262464.4:p.Gln1256Glu
|
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ENST00000262464.8:c.3766C>G
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ENSP00000262464.4:p.Gln1256Glu
|
|
ENST00000507835.5:c.316C>G
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ENSP00000426839.1:p.Gln106Glu
|
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ENST00000508053.5:c.3766C>G
|
ENSP00000424571.1:p.Gln1256Glu
|
|
ENST00000508989.5:c.3667C>G
|
ENSP00000425596.1:p.Gln1223Glu
|
|
ENST00000619499.4:c.3763C>G
|
ENSP00000482132.1:p.Gln1255Glu
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NM_001999.3:c.3766C>G
|
NP_001990.2:p.Gln1256Glu
|
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XM_017009228.2:c.3613C>G
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XP_016864717.1:p.Gln1205Glu
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NM_001999.4:c.3766C>G
MANE Select
|
NP_001990.2:p.Gln1256Glu
|
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