ENST00000382103.7:c.1026+473A>G
MANE Select
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ENSP00000371535.2:n.1026+473A>G
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ENST00000680581.1:c.1026+473A>G
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ENSP00000506483.1:n.1026+473A>G
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|
ENST00000680824.1:n.2242+473A>G
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|
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ENST00000681071.1:n.1318+473A>G
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|
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ENST00000681341.1:n.2167+473A>G
|
|
|
ENST00000681948.1:c.1281+473A>G
|
ENSP00000505991.1:n.1281+473A>G
|
|
ENST00000358971.7:c.*824+473A>G
|
ENSP00000351857.3:n.*824+473A>G
|
|
ENST00000382103.6:c.1026+473A>G
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ENSP00000371535.2:n.1026+473A>G
|
|
ENST00000503150.1:c.308+473A>G
|
|
|
ENST00000505513.1:n.326+473A>G
|
|
|
ENST00000514585.5:c.*727+473A>G
|
ENSP00000421880.1:n.*727+473A>G
|
|
NM_016955.3:c.1026+473A>G
|
NP_058651.3:n.1026+473A>G
|
|
XM_005248168.2:c.789+473A>G
|
XP_005248225.1:n.789+473A>G
|
|
XM_006713965.2:c.846+473A>G
|
XP_006714028.1:n.846+473A>G
|
|
XM_011513846.1:c.1023+473A>G
|
XP_011512148.1:n.1023+473A>G
|
|
XM_011513847.1:c.993+473A>G
|
XP_011512149.1:n.993+473A>G
|
|
XM_011513848.1:c.846+473A>G
|
XP_011512150.1:n.846+473A>G
|
|
XM_011513846.2:c.1023+473A>G
|
XP_011512148.1:n.1023+473A>G
|
|
XM_011513847.2:c.993+473A>G
|
XP_011512149.1:n.993+473A>G
|
|
XM_017008277.1:c.1281+473A>G
|
XP_016863766.1:n.1281+473A>G
|
|
XM_017008278.1:c.603+473A>G
|
XP_016863767.1:n.603+473A>G
|
|
NM_016955.4:c.1026+473A>G
MANE Select
|
NP_058651.3:n.1026+473A>G
|
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