ENST00000645828.1:n.2732A>C
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ENST00000651671.1:c.4925A>C
MANE Select
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ENSP00000498587.1:p.Asp1642Ala
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ENST00000679595.1:c.4925A>C
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ENSP00000506241.1:p.Asp1642Ala
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ENST00000680133.1:c.4811A>C
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ENSP00000505319.1:p.Asp1604Ala
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ENST00000680218.1:c.4805A>C
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ENSP00000505339.1:p.Asp1602Ala
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ENST00000680668.1:c.4811A>C
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ENSP00000506336.1:p.Asp1604Ala
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ENST00000680778.1:c.2522A>C
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ENSP00000506033.1:p.Asp841Ala
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ENST00000680924.1:c.*2325A>C
|
ENSP00000506031.1:n.*2325A>C
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ENST00000681135.1:c.*2534A>C
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ENSP00000506636.1:n.*2534A>C
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ENST00000681298.1:n.1738A>C
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ENST00000681454.1:c.*4161A>C
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ENSP00000505763.1:n.*4161A>C
|
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ENST00000277541.6:c.4925A>C
|
ENSP00000277541.6:p.Asp1642Ala
|
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ENST00000494783.1:n.80A>C
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|
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NM_017617.3:c.4925A>C
|
NP_060087.3:p.Asp1642Ala
|
|
XM_011518717.1:c.4226A>C
|
XP_011517019.1:p.Asp1409Ala
|
|
NM_017617.5:c.4925A>C
MANE Select
|
NP_060087.3:p.Asp1642Ala
|
|
XM_011518717.2:c.4202A>C
|
XP_011517019.2:p.Asp1401Ala
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