ENST00000645828.1:n.2726C>G
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ENST00000651671.1:c.4919C>G
MANE Select
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ENSP00000498587.1:p.Ala1640Gly
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ENST00000679595.1:c.4919C>G
|
ENSP00000506241.1:p.Ala1640Gly
|
|
ENST00000680133.1:c.4805C>G
|
ENSP00000505319.1:p.Ala1602Gly
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ENST00000680218.1:c.4799C>G
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ENSP00000505339.1:p.Ala1600Gly
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ENST00000680668.1:c.4805C>G
|
ENSP00000506336.1:p.Ala1602Gly
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ENST00000680778.1:c.2516C>G
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ENSP00000506033.1:p.Ala839Gly
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ENST00000680924.1:c.*2319C>G
|
ENSP00000506031.1:n.*2319C>G
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ENST00000681135.1:c.*2528C>G
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ENSP00000506636.1:n.*2528C>G
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ENST00000681298.1:n.1732C>G
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ENST00000681454.1:c.*4155C>G
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ENSP00000505763.1:n.*4155C>G
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ENST00000277541.6:c.4919C>G
|
ENSP00000277541.6:p.Ala1640Gly
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ENST00000494783.1:n.74C>G
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|
|
NM_017617.3:c.4919C>G
|
NP_060087.3:p.Ala1640Gly
|
|
XM_011518717.1:c.4220C>G
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XP_011517019.1:p.Ala1407Gly
|
|
NM_017617.5:c.4919C>G
MANE Select
|
NP_060087.3:p.Ala1640Gly
|
|
XM_011518717.2:c.4196C>G
|
XP_011517019.2:p.Ala1399Gly
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