ENST00000340253.10:c.1835T>G
MANE Select
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ENSP00000342023.6:p.Val612Gly
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ENST00000296701.10:c.1835T>G
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ENSP00000296701.6:p.Val612Gly
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ENST00000340253.9:c.1835T>G
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ENSP00000342023.5:p.Val612Gly
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ENST00000394370.7:c.1835T>G
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ENSP00000377895.3:p.Val612Gly
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ENST00000513826.1:c.1835T>G
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ENSP00000426410.1:p.Val612Gly
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ENST00000514832.1:n.466T>G
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|
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NM_001271723.1:c.1835T>G
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NP_001258652.1:p.Val612Gly
|
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NM_030793.4:c.1835T>G
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NP_110420.3:p.Val612Gly
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XM_005268513.1:c.1835T>G
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XP_005268570.1:p.Val612Gly
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XM_006714797.1:c.1835T>G
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XP_006714860.1:p.Val612Gly
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XM_011537683.1:c.737T>G
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XP_011535985.1:p.Val246Gly
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|
XM_011537684.1:c.635T>G
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XP_011535986.1:p.Val212Gly
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NM_205836.2:c.1835T>G
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NP_995308.1:p.Val612Gly
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XM_006714797.2:c.1835T>G
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XP_006714860.1:p.Val612Gly
|
|
XM_011537684.3:c.635T>G
|
XP_011535986.1:p.Val212Gly
|
|
XM_017009899.1:c.737T>G
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XP_016865388.1:p.Val246Gly
|
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XM_017009900.2:c.635T>G
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XP_016865389.1:p.Val212Gly
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XM_017009901.2:c.737T>G
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XP_016865390.1:p.Val246Gly
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XM_017009902.2:c.635T>G
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XP_016865391.1:p.Val212Gly
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XM_024446223.1:c.1835T>G
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XP_024301991.1:p.Val612Gly
|
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XR_001742284.1:n.1981T>G
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NM_030793.5:c.1835T>G
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NP_110420.3:p.Val612Gly
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NM_205836.3:c.1835T>G
MANE Select
|
NP_995308.1:p.Val612Gly
|
|
NM_001271723.2:c.1835T>G
|
NP_001258652.1:p.Val612Gly
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