ENST00000344209.10:c.1181A>G
MANE Select
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ENSP00000345667.5:p.Glu394Gly
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ENST00000460554.2:n.1131A>G
|
|
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ENST00000642615.1:c.*364A>G
|
ENSP00000495499.1:n.*364A>G
|
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ENST00000273691.7:c.1049A>G
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ENSP00000273691.3:p.Glu350Gly
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ENST00000344209.9:c.1181A>G
|
ENSP00000345667.5:p.Glu394Gly
|
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ENST00000393631.5:c.914A>G
|
ENSP00000377251.1:p.Glu305Gly
|
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ENST00000460554.1:n.1283A>G
|
|
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ENST00000462014.1:c.1085A>G
|
ENSP00000419414.1:p.Glu362Gly
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NM_001199799.1:c.1181A>G
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NP_001186728.1:p.Glu394Gly
|
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NM_001199800.1:c.914A>G
|
NP_001186729.1:p.Glu305Gly
|
|
NM_175924.3:c.1049A>G
|
NP_787120.1:p.Glu350Gly
|
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XM_005247389.3:c.1085A>G
|
XP_005247446.1:p.Glu362Gly
|
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XM_011512738.1:c.1181A>G
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XP_011511040.1:p.Glu394Gly
|
|
XM_011512739.1:c.644A>G
|
XP_011511041.1:p.Glu215Gly
|
|
XM_005247389.4:c.1085A>G
|
XP_005247446.1:p.Glu362Gly
|
|
XM_011512738.2:c.1181A>G
|
XP_011511040.1:p.Glu394Gly
|
|
XM_011512739.2:c.644A>G
|
XP_011511041.1:p.Glu215Gly
|
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NM_001199799.2:c.1181A>G
MANE Select
|
NP_001186728.1:p.Glu394Gly
|
|
NM_001199800.2:c.914A>G
|
NP_001186729.1:p.Glu305Gly
|
|
NM_175924.4:c.1049A>G
|
NP_787120.1:p.Glu350Gly
|
|