ENST00000261769.10:c.2081T>G
MANE Select
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ENSP00000261769.4:p.Val694Gly
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ENST00000261769.9:c.2081T>G
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ENSP00000261769.4:p.Val694Gly
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ENST00000422392.6:c.1898T>G
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ENSP00000414946.2:p.Val633Gly
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ENST00000562118.1:n.299T>G
|
|
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ENST00000562836.5:n.2152T>G
|
|
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ENST00000566510.5:c.*747T>G
|
ENSP00000458139.1:n.*747T>G
|
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ENST00000566612.5:c.*321T>G
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ENSP00000454782.1:n.*321T>G
|
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ENST00000611625.4:c.2144T>G
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ENSP00000481063.1:p.Val715Gly
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ENST00000612417.4:c.1830+1424T>G
|
ENSP00000478360.1:n.1830+1424T>G
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ENST00000621016.4:c.1865+1389T>G
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ENSP00000480664.1:n.1865+1389T>G
|
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NM_004360.3:c.2081T>G , LRG_301t1:c.2081T>G
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NP_004351.1:p.Val694Gly
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XM_011523488.1:c.1346T>G
|
XP_011521790.1:p.Val449Gly
|
|
XM_011523489.1:c.1346T>G
|
XP_011521791.1:p.Val449Gly
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NM_001317184.1:c.1898T>G
|
NP_001304113.1:p.Val633Gly
|
|
NM_001317185.1:c.533T>G
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NP_001304114.1:p.Val178Gly
|
|
NM_001317186.1:c.116T>G
|
NP_001304115.1:p.Val39Gly
|
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NM_004360.4:c.2081T>G
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NP_004351.1:p.Val694Gly
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NM_004360.5:c.2081T>G
MANE Select
|
NP_004351.1:p.Val694Gly
|
|
NM_001317184.2:c.1898T>G
|
NP_001304113.1:p.Val633Gly
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|
NM_001317185.2:c.533T>G
|
NP_001304114.1:p.Val178Gly
|
|
NM_001317186.2:c.116T>G
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NP_001304115.1:p.Val39Gly
|
|