ENST00000270301.12:c.3148C>T
|
ENSP00000270301.6:p.Leu1050=
|
|
ENST00000401500.7:c.3148C>T
MANE Select
|
ENSP00000384792.1:p.Leu1050=
|
|
ENST00000587391.6:c.*2423C>T
|
ENSP00000465525.1:n.*2423C>T
|
|
ENST00000679357.1:c.938C>T
|
|
|
ENST00000679422.1:c.827C>T
|
|
|
ENST00000679682.1:c.3133C>T
|
ENSP00000506226.1:p.Leu1045=
|
|
ENST00000679714.1:c.3142C>T
|
ENSP00000506627.1:p.Leu1048=
|
|
ENST00000679757.1:c.2797C>T
|
ENSP00000505158.1:p.Leu933=
|
|
ENST00000679858.1:c.*2530C>T
|
ENSP00000505655.1:n.*2530C>T
|
|
ENST00000680211.1:c.-252C>T
|
ENSP00000506102.1:n.-252C>T
|
|
ENST00000680349.1:n.1131C>T
|
|
|
ENST00000680403.1:c.3148C>T
|
ENSP00000505677.1:p.Leu1050=
|
|
ENST00000680564.1:c.2972-658C>T
|
ENSP00000505582.1:n.2972-658C>T
|
|
ENST00000680590.1:c.*1543C>T
|
ENSP00000505350.1:n.*1543C>T
|
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ENST00000680739.1:c.66C>T
|
|
|
ENST00000680773.1:n.1064C>T
|
|
|
ENST00000680806.1:c.*1866C>T
|
ENSP00000506418.1:n.*1866C>T
|
|
ENST00000680997.1:n.495C>T
|
|
|
ENST00000681088.1:c.810C>T
|
|
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ENST00000681608.1:n.96C>T
|
|
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ENST00000681625.1:c.*480C>T
|
ENSP00000505555.1:n.*480C>T
|
|
ENST00000270301.11:c.3148C>T
|
ENSP00000270301.6:p.Leu1050=
|
|
ENST00000401500.6:c.3148C>T
|
ENSP00000384792.1:p.Leu1050=
|
|
ENST00000587391.5:c.*2423C>T
|
ENSP00000465525.1:n.*2423C>T
|
|
NM_001083961.1:c.3148C>T
|
NP_001077430.1:p.Leu1050=
|
|
NM_173636.4:c.3148C>T
|
NP_775907.4:p.Leu1050=
|
|
XM_005258809.2:c.3037C>T
|
XP_005258866.1:p.Leu1013=
|
|
XM_011526837.1:c.3133C>T
|
XP_011525139.1:p.Leu1045=
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XM_011526838.1:c.2972-658C>T
|
XP_011525140.1:n.2972-658C>T
|
|
XM_011526839.1:c.2797C>T
|
XP_011525141.1:p.Leu933=
|
|
XM_011526840.1:c.2140C>T
|
XP_011525142.1:p.Leu714=
|
|
XM_011526841.1:c.1726C>T
|
XP_011525143.1:p.Leu576=
|
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XM_011526842.1:c.1579C>T
|
XP_011525144.1:p.Leu527=
|
|
XM_011526843.1:c.895C>T
|
XP_011525145.1:p.Leu299=
|
|
XM_011526844.1:c.895C>T
|
XP_011525146.1:p.Leu299=
|
|
XM_011526840.2:c.2140C>T
|
XP_011525142.1:p.Leu714=
|
|
XM_011526841.2:c.1726C>T
|
XP_011525143.1:p.Leu576=
|
|
XM_011526844.2:c.895C>T
|
XP_011525146.1:p.Leu299=
|
|
XM_017026665.1:c.3148C>T
|
XP_016882154.1:p.Leu1050=
|
|
NM_001083961.2:c.3148C>T
MANE Select
|
NP_001077430.1:p.Leu1050=
|
|
NM_173636.5:c.3148C>T
|
NP_775907.4:p.Leu1050=
|
|