ENST00000336079.8:c.1842T>G
MANE Select
|
ENSP00000336725.3:p.Ser614Arg
|
|
ENST00000336079.7:c.1842T>G
|
ENSP00000336725.3:p.Ser614Arg
|
|
ENST00000360160.8:c.1842T>G
|
ENSP00000353284.4:p.Ser614Arg
|
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NM_001122665.2:c.1842T>G
|
NP_001116137.1:p.Ser614Arg
|
|
NM_001302552.1:c.1833T>G
|
NP_001289481.1:p.Ser611Arg
|
|
NM_004660.4:c.1842T>G
|
NP_004651.2:p.Ser614Arg
|
|
XM_006724878.1:c.1773T>G
|
XP_006724941.1:p.Ser591Arg
|
|
NM_001122665.3:c.1842T>G
|
NP_001116137.1:p.Ser614Arg
|
|
NM_001302552.2:c.1833T>G
|
NP_001289481.1:p.Ser611Arg
|
|
NM_001324195.1:c.1773T>G
|
NP_001311124.1:p.Ser591Arg
|
|
NR_136716.1:n.2311T>G
|
|
|
NR_136717.1:n.2073T>G
|
|
|
NR_136718.1:n.2391T>G
|
|
|
NR_136719.1:n.2181T>G
|
|
|
NR_136720.1:n.2242T>G
|
|
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NR_136721.1:n.1904T>G
|
|
|
NR_136722.1:n.1988T>G
|
|
|
NR_136723.1:n.2306T>G
|
|
|
NR_136724.1:n.2226T>G
|
|
|
XR_001756014.2:n.2006T>G
|
|
|
NM_004660.5:c.1842T>G
MANE Select
|
NP_004651.2:p.Ser614Arg
|
|
NM_001302552.3:c.1833T>G
|
NP_001289481.1:p.Ser611Arg
|
|
NM_001324195.2:c.1773T>G
|
NP_001311124.1:p.Ser591Arg
|
|
NR_136716.2:n.2229T>G
|
|
|
NR_136717.2:n.1991T>G
|
|
|
NR_136718.2:n.2309T>G
|
|
|
NR_136719.2:n.2099T>G
|
|
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NR_136720.2:n.2160T>G
|
|
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NR_136721.2:n.1894T>G
|
|
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