ENST00000651671.1:c.6137T>G
MANE Select
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ENSP00000498587.1:p.Val2046Gly
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ENST00000679595.1:c.*1177T>G
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ENSP00000506241.1:n.*1177T>G
|
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ENST00000679969.1:n.2733T>G
|
|
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ENST00000680003.1:n.2469T>G
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|
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ENST00000680133.1:c.6023T>G
|
ENSP00000505319.1:p.Val2008Gly
|
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ENST00000680218.1:c.6017T>G
|
ENSP00000505339.1:p.Val2006Gly
|
|
ENST00000680668.1:c.6023T>G
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ENSP00000506336.1:p.Val2008Gly
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ENST00000680778.1:c.3734T>G
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ENSP00000506033.1:p.Val1245Gly
|
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ENST00000680924.1:c.*3537T>G
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ENSP00000506031.1:n.*3537T>G
|
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ENST00000681135.1:c.*3746T>G
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ENSP00000506636.1:n.*3746T>G
|
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ENST00000681298.1:n.4242T>G
|
|
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ENST00000681454.1:c.*5373T>G
|
ENSP00000505763.1:n.*5373T>G
|
|
ENST00000277541.6:c.6137T>G
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ENSP00000277541.6:p.Val2046Gly
|
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NM_017617.3:c.6137T>G
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NP_060087.3:p.Val2046Gly
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XM_011518717.1:c.5438T>G
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XP_011517019.1:p.Val1813Gly
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NM_017617.5:c.6137T>G
MANE Select
|
NP_060087.3:p.Val2046Gly
|
|
XM_011518717.2:c.5414T>G
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XP_011517019.2:p.Val1805Gly
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