ENST00000426508.7:c.4361T>G
MANE Select
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ENSP00000406012.2:p.Val1454Gly
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ENST00000361339.9:c.1943T>G
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ENSP00000354895.5:p.Val648Gly
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ENST00000397417.6:c.*2799T>G
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ENSP00000380562.2:n.*2799T>G
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ENST00000426508.6:c.4361T>G
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ENSP00000406012.2:p.Val1454Gly
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ENST00000565298.5:n.4185T>G
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|
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NM_014714.3:c.4361T>G
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NP_055529.2:p.Val1454Gly
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XM_006720989.2:c.4361T>G
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XP_006721052.1:p.Val1454Gly
|
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XM_006720990.2:c.4361T>G
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XP_006721053.1:p.Val1454Gly
|
|
XM_006720991.2:c.4361T>G
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XP_006721054.1:p.Val1454Gly
|
|
XM_006720992.2:c.1994T>G
|
XP_006721055.1:p.Val665Gly
|
|
XM_011522766.1:c.4115T>G
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XP_011521068.1:p.Val1372Gly
|
|
XM_011522767.1:c.3386T>G
|
XP_011521069.1:p.Val1129Gly
|
|
XM_006720990.3:c.4361T>G
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XP_006721053.1:p.Val1454Gly
|
|
XM_006720991.3:c.4361T>G
|
XP_006721054.1:p.Val1454Gly
|
|
XM_006720992.3:c.1994T>G
|
XP_006721055.1:p.Val665Gly
|
|
XM_011522766.3:c.4115T>G
|
XP_011521068.1:p.Val1372Gly
|
|
XM_011522767.2:c.3386T>G
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XP_011521069.1:p.Val1129Gly
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|
XM_017023910.1:c.4361T>G
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XP_016879399.1:p.Val1454Gly
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|
XM_017023911.1:c.2546T>G
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XP_016879400.1:p.Val849Gly
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NM_014714.4:c.4361T>G
MANE Select
|
NP_055529.2:p.Val1454Gly
|
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