ENST00000302328.9:c.2615G=
MANE Select
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ENSP00000307599.3:p.Gly872=
|
|
ENST00000668754.1:c.2615G=
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ENSP00000499569.1:p.Gly872=
|
|
ENST00000675223.1:c.2615G=
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ENSP00000502481.1:p.Gly872=
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|
ENST00000675672.1:c.2615G=
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ENSP00000502446.1:p.Gly872=
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|
ENST00000675892.1:c.2435G=
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ENSP00000502318.1:p.Gly812=
|
|
ENST00000676045.1:c.2659G=
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ENSP00000501685.1:n.2659G=
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|
ENST00000676176.1:c.2234G=
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ENSP00000501891.1:p.Gly745=
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|
ENST00000302328.7:c.2615G=
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ENSP00000307599.3:p.Gly872=
|
|
ENST00000444237.2:c.2615G=
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ENSP00000408028.2:p.Gly872=
|
|
ENST00000456224.7:c.2615G=
|
ENSP00000416757.3:p.Gly872=
|
|
NM_001287223.1:c.2615G=
|
NP_001274152.1:p.Gly872=
|
|
NM_014139.2:c.2615G=
|
NP_054858.2:p.Gly872=
|
|
XM_011533320.1:c.2615G=
|
XP_011531622.1:p.Gly872=
|
|
XM_011533321.1:c.1952G=
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XP_011531623.1:p.Gly651=
|
|
XM_011533322.1:c.1163G=
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XP_011531624.1:p.Gly388=
|
|
NM_001349253.1:c.2615G=
|
NP_001336182.1:p.Gly872=
|
|
XM_011533321.2:c.1952G=
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XP_011531623.1:p.Gly651=
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|
XM_017005647.1:c.2990G=
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XP_016861136.1:p.Gly997=
|
|
XM_017005648.1:c.2417G=
|
XP_016861137.1:p.Gly806=
|
|
XM_017005650.1:c.2615G=
|
XP_016861139.1:p.Gly872=
|
|
XM_017005651.1:c.2342G=
|
XP_016861140.1:p.Gly781=
|
|
XM_017005652.1:c.2615G=
|
XP_016861141.1:p.Gly872=
|
|
XM_017005653.1:c.1019G=
|
XP_016861142.1:p.Gly340=
|
|
NM_001349253.2:c.2615G=
MANE Select
|
NP_001336182.1:p.Gly872=
|
|
NM_014139.3:c.2615G=
|
NP_054858.2:p.Gly872=
|
|