ENST00000359271.4:c.524C>G
MANE Select
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ENSP00000352216.2:p.Ala175Gly
|
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ENST00000359271.3:c.524C>G
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ENSP00000352216.2:p.Ala175Gly
|
|
NM_030777.3:c.524C>G
|
NP_110404.1:p.Ala175Gly
|
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XM_011529060.1:c.587C>G
|
XP_011527362.1:p.Ala196Gly
|
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XM_011529061.1:c.533C>G
|
XP_011527363.1:p.Ala178Gly
|
|
XM_011529062.1:c.587C>G
|
XP_011527364.1:p.Ala196Gly
|
|
XM_011529063.1:c.587C>G
|
XP_011527365.1:p.Ala196Gly
|
|
XM_011529064.1:c.587C>G
|
XP_011527366.1:p.Ala196Gly
|
|
XM_011529065.1:c.587C>G
|
XP_011527367.1:p.Ala196Gly
|
|
XR_936641.1:n.723C>G
|
|
|
XM_011529060.2:c.587C>G
|
XP_011527362.1:p.Ala196Gly
|
|
XM_011529061.2:c.533C>G
|
XP_011527363.1:p.Ala178Gly
|
|
XM_011529062.2:c.587C>G
|
XP_011527364.1:p.Ala196Gly
|
|
XM_011529063.2:c.587C>G
|
XP_011527365.1:p.Ala196Gly
|
|
XM_011529064.2:c.587C>G
|
XP_011527366.1:p.Ala196Gly
|
|
XM_011529065.2:c.587C>G
|
XP_011527367.1:p.Ala196Gly
|
|
XM_017028087.2:c.524C>G
|
XP_016883576.1:p.Ala175Gly
|
|
XR_936641.2:n.710C>G
|
|
|
NM_030777.4:c.524C>G
MANE Select
|
NP_110404.1:p.Ala175Gly
|
|