ENST00000382103.7:c.1026G=
MANE Select
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ENSP00000371535.2:p.Lys342=
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|
ENST00000680581.1:c.1026G=
|
ENSP00000506483.1:p.Lys342=
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|
ENST00000680824.1:n.2242G=
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ENST00000681071.1:n.1318G=
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|
|
ENST00000681341.1:n.2167G=
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|
|
ENST00000681948.1:c.1281G=
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ENSP00000505991.1:p.Lys427=
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|
ENST00000358971.7:c.*824G=
|
ENSP00000351857.3:n.*824G=
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|
ENST00000382103.6:c.1026G=
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ENSP00000371535.2:p.Lys342=
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ENST00000503150.1:c.308G=
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|
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ENST00000505513.1:n.326G=
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|
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ENST00000514585.5:c.*727G=
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ENSP00000421880.1:n.*727G=
|
|
NM_016955.3:c.1026G=
|
NP_058651.3:p.Lys342=
|
|
XM_005248168.2:c.789G=
|
XP_005248225.1:p.Lys263=
|
|
XM_006713965.2:c.846G=
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XP_006714028.1:p.Lys282=
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|
XM_011513846.1:c.1023G=
|
XP_011512148.1:p.Lys341=
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|
XM_011513847.1:c.993G=
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XP_011512149.1:p.Lys331=
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|
XM_011513848.1:c.846G=
|
XP_011512150.1:p.Lys282=
|
|
XM_011513846.2:c.1023G=
|
XP_011512148.1:p.Lys341=
|
|
XM_011513847.2:c.993G=
|
XP_011512149.1:p.Lys331=
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|
XM_017008277.1:c.1281G=
|
XP_016863766.1:p.Lys427=
|
|
XM_017008278.1:c.603G=
|
XP_016863767.1:p.Lys201=
|
|
NM_016955.4:c.1026G=
MANE Select
|
NP_058651.3:p.Lys342=
|
|