ENST00000262367.10:c.5434A>G
MANE Select
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ENSP00000262367.5:p.Thr1812Ala
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ENST00000262367.9:c.5434A>G
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ENSP00000262367.5:p.Thr1812Ala
|
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ENST00000382070.7:c.5320A>G
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ENSP00000371502.3:p.Thr1774Ala
|
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NM_001079846.1:c.5320A>G
|
NP_001073315.1:p.Thr1774Ala
|
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NM_004380.2:c.5434A>G
|
NP_004371.2:p.Thr1812Ala
|
|
XM_005255124.3:c.5389A>G
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XP_005255181.1:p.Thr1797Ala
|
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XM_005255125.3:c.5017A>G
|
XP_005255182.1:p.Thr1673Ala
|
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XM_006720848.2:c.5173A>G
|
XP_006720911.1:p.Thr1725Ala
|
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XM_011522380.1:c.5380A>G
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XP_011520682.1:p.Thr1794Ala
|
|
XM_011522381.1:c.4681A>G
|
XP_011520683.1:p.Thr1561Ala
|
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XM_005255124.4:c.5389A>G
|
XP_005255181.1:p.Thr1797Ala
|
|
XM_005255125.4:c.5017A>G
|
XP_005255182.1:p.Thr1673Ala
|
|
XM_006720848.3:c.5173A>G
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XP_006720911.1:p.Thr1725Ala
|
|
XM_011522381.2:c.4681A>G
|
XP_011520683.1:p.Thr1561Ala
|
|
XM_017022944.1:c.5428A>G
|
XP_016878433.1:p.Thr1810Ala
|
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NM_004380.3:c.5434A>G
MANE Select
|
NP_004371.2:p.Thr1812Ala
|
|