ENST00000298910.12:c.5999T>G
MANE Select
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ENSP00000298910.7:p.Val2000Gly
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ENST00000679360.1:c.*4908T>G
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ENSP00000505368.1:n.*4908T>G
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ENST00000679532.1:c.1773T>G
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ENST00000680018.1:c.1444T>G
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ENSP00000505347.1:n.1444T>G
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ENST00000680422.1:c.1644T>G
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ENST00000680425.1:c.1166T>G
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ENSP00000506459.1:n.1166T>G
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ENST00000680453.1:c.1456T>G
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ENST00000680790.1:c.5744T>G
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ENSP00000505335.1:p.Val1915Gly
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ENST00000681136.1:n.1983T>G
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ENST00000681696.1:c.1682T>G
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ENSP00000505871.1:p.Val561Gly
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ENST00000298910.11:c.5999T>G
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ENSP00000298910.7:p.Val2000Gly
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ENST00000430804.5:c.3295T>G
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ENST00000479187.5:n.2680T>G
|
|
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NM_198578.3:c.5999T>G
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NP_940980.3:p.Val2000Gly
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XM_005268629.2:c.5999T>G
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XP_005268686.1:p.Val2000Gly
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XM_011537877.1:c.5999T>G
|
XP_011536179.1:p.Val2000Gly
|
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XM_011537878.1:c.5999T>G
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XP_011536180.1:p.Val2000Gly
|
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XM_011537879.1:c.4796T>G
|
XP_011536181.1:p.Val1599Gly
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XM_005268629.4:c.5999T>G
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XP_005268686.1:p.Val2000Gly
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XM_011537877.3:c.5999T>G
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XP_011536179.1:p.Val2000Gly
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XM_017018787.1:c.2915T>G
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XP_016874276.1:p.Val972Gly
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XM_017018788.2:c.2261T>G
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XP_016874277.1:p.Val754Gly
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XM_024448833.1:c.4796T>G
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XP_024304601.1:p.Val1599Gly
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NM_198578.4:c.5999T>G
MANE Select
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NP_940980.4:p.Val2000Gly
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