ENST00000302328.9:c.2708T>G
MANE Select
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ENSP00000307599.3:p.Val903Gly
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ENST00000668754.1:c.2708T>G
|
ENSP00000499569.1:p.Val903Gly
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|
ENST00000675223.1:c.2708T>G
|
ENSP00000502481.1:p.Val903Gly
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ENST00000675672.1:c.2708T>G
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ENSP00000502446.1:p.Val903Gly
|
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ENST00000675892.1:c.2528T>G
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ENSP00000502318.1:p.Val843Gly
|
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ENST00000676045.1:c.2752T>G
|
ENSP00000501685.1:n.2752T>G
|
|
ENST00000676176.1:c.2327T>G
|
ENSP00000501891.1:p.Val776Gly
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ENST00000302328.7:c.2708T>G
|
ENSP00000307599.3:p.Val903Gly
|
|
ENST00000444237.2:c.2708T>G
|
ENSP00000408028.2:p.Val903Gly
|
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ENST00000456224.7:c.2708T>G
|
ENSP00000416757.3:p.Val903Gly
|
|
NM_001287223.1:c.2708T>G
|
NP_001274152.1:p.Val903Gly
|
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NM_014139.2:c.2708T>G
|
NP_054858.2:p.Val903Gly
|
|
XM_011533320.1:c.2708T>G
|
XP_011531622.1:p.Val903Gly
|
|
XM_011533321.1:c.2045T>G
|
XP_011531623.1:p.Val682Gly
|
|
XM_011533322.1:c.1256T>G
|
XP_011531624.1:p.Val419Gly
|
|
NM_001349253.1:c.2708T>G
|
NP_001336182.1:p.Val903Gly
|
|
XM_011533321.2:c.2045T>G
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XP_011531623.1:p.Val682Gly
|
|
XM_017005647.1:c.3083T>G
|
XP_016861136.1:p.Val1028Gly
|
|
XM_017005648.1:c.2510T>G
|
XP_016861137.1:p.Val837Gly
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|
XM_017005650.1:c.2708T>G
|
XP_016861139.1:p.Val903Gly
|
|
XM_017005651.1:c.2435T>G
|
XP_016861140.1:p.Val812Gly
|
|
XM_017005652.1:c.2708T>G
|
XP_016861141.1:p.Val903Gly
|
|
XM_017005653.1:c.1112T>G
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XP_016861142.1:p.Val371Gly
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NM_001349253.2:c.2708T>G
MANE Select
|
NP_001336182.1:p.Val903Gly
|
|
NM_014139.3:c.2708T>G
|
NP_054858.2:p.Val903Gly
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