ENST00000359595.8:c.293A>C
MANE Select
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ENSP00000352606.4:p.Glu98Ala
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ENST00000359595.7:c.293A>C
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ENSP00000352606.3:p.Glu98Ala
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ENST00000558770.5:c.293A>C
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ENSP00000456458.1:p.Glu98Ala
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ENST00000562281.1:c.293A>C
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ENSP00000456985.1:p.Glu98Ala
|
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ENST00000562889.5:c.479A>C
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ENSP00000457180.1:p.Glu160Ala
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ENST00000563808.1:n.395A>C
|
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NM_001307952.1:c.479A>C
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NP_001294881.1:p.Glu160Ala
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NM_178232.2:c.293A>C
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NP_839946.1:p.Glu98Ala
|
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NM_178232.3:c.293A>C
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NP_839946.1:p.Glu98Ala
|
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XM_011521261.1:c.425A>C
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XP_011519563.1:p.Glu142Ala
|
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XR_243204.1:n.508A>C
|
|
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XR_931756.1:n.614A>C
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|
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XM_017021934.2:c.479A>C
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XP_016877423.1:p.Glu160Ala
|
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XM_017021935.2:c.-87A>C
|
XP_016877424.1:n.-87A>C
|
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XM_017021936.2:c.-87A>C
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XP_016877425.1:n.-87A>C
|
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XR_001751098.2:n.626A>C
|
|
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XR_931756.3:n.627A>C
|
|
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NM_001307952.2:c.479A>C
|
NP_001294881.1:p.Glu160Ala
|
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NM_178232.4:c.293A>C
MANE Select
|
NP_839946.1:p.Glu98Ala
|
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