ENST00000366159.9:n.282A>C
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|
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ENST00000437813.8:c.248A>C
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ENSP00000513672.1:p.Glu83Ala
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ENST00000440083.7:c.248A>C
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ENSP00000413224.3:p.Glu83Ala
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ENST00000535958.2:c.*75A>C
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ENSP00000513673.1:n.*75A>C
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ENST00000698339.1:c.248A>C
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ENSP00000513670.1:p.Glu83Ala
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ENST00000698340.1:c.248A>C
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ENSP00000513671.1:p.Glu83Ala
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ENST00000162749.7:c.248A>C
MANE Select
|
ENSP00000162749.2:p.Glu83Ala
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ENST00000162749.6:c.248A>C
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ENSP00000162749.2:p.Glu83Ala
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|
ENST00000366159.8:c.248A>C
|
ENSP00000380389.3:p.Glu83Ala
|
|
ENST00000437813.7:n.209A>C
|
|
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ENST00000440083.6:c.248A>C
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ENSP00000413224.2:p.Glu83Ala
|
|
ENST00000534885.5:c.94A>C
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ENSP00000441803.1:p.Ser32Arg
|
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ENST00000535958.1:n.494A>C
|
|
|
ENST00000536194.1:c.221A>C
|
ENSP00000442919.1:p.Glu74Ala
|
|
ENST00000539372.5:c.248A>C
|
ENSP00000442059.1:p.Glu83Ala
|
|
ENST00000540022.5:c.193+280A>C
|
ENSP00000438343.1:n.193+280A>C
|
|
ENST00000543048.5:c.214+34A>C
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ENSP00000439981.1:n.214+34A>C
|
|
ENST00000543995.5:c.193+280A>C
|
ENSP00000442405.1:n.193+280A>C
|
|
NM_001065.3:c.248A>C , LRG_193t1:c.248A>C
|
NP_001056.1:p.Glu83Ala
|
|
NM_001346091.1:c.-77A>C
|
NP_001333020.1:n.-77A>C
|
|
NM_001346092.1:c.-330A>C
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NP_001333021.1:n.-330A>C
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|
NR_144351.1:n.551A>C
|
|
|
NM_001065.4:c.248A>C
MANE Select
|
NP_001056.1:p.Glu83Ala
|
|
NM_001346091.2:c.-77A>C
|
NP_001333020.1:n.-77A>C
|
|
NM_001346092.2:c.-330A>C
|
NP_001333021.1:n.-330A>C
|
|
NR_144351.2:n.510A>C
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