ENST00000296589.9:c.579G=
MANE Select
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ENSP00000296589.4:p.Leu193=
|
|
ENST00000296589.8:c.579G=
|
ENSP00000296589.4:p.Leu193=
|
|
ENST00000382102.7:c.579G=
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ENSP00000371534.3:p.Leu193=
|
|
ENST00000505056.1:n.381G=
|
|
|
ENST00000509381.1:c.563-9496G=
|
ENSP00000421100.1:n.563-9496G=
|
|
ENST00000510600.1:c.54G=
|
ENSP00000424010.1:p.Leu18=
|
|
NM_001012509.3:c.579G=
|
NP_001012527.1:p.Leu193=
|
|
NM_001297417.2:c.563-9496G=
|
NP_001284346.2:n.563-9496G=
|
|
NM_016180.4:c.579G=
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NP_057264.3:p.Leu193=
|
|
XM_011514051.1:c.177G=
|
XP_011512353.1:p.Leu59=
|
|
XM_011514052.1:c.579G=
|
XP_011512354.1:p.Leu193=
|
|
XR_925620.1:n.1396G=
|
|
|
NM_016180.5:c.579G=
MANE Select
|
NP_057264.4:p.Leu193=
|
|
NM_001012509.4:c.579G=
|
NP_001012527.2:p.Leu193=
|
|
NM_001297417.3:c.563-9496G=
|
NP_001284346.2:n.563-9496G=
|
|
NM_001297417.4:c.563-9496G=
|
NP_001284346.2:n.563-9496G=
|
|