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ENST00000360822.8:c.2979T=
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ENSP00000354065.4:p.Leu993=
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ENST00000416449.6:c.3573T=
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ENSP00000400395.2:p.Leu1191=
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ENST00000479584.2:n.1916T=
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ENST00000684780.1:n.3959T=
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ENST00000685866.1:c.*1496T=
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ENSP00000509484.1:n.*1496T=
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ENST00000686376.1:c.3749T=
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ENSP00000510021.1:n.3749T=
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ENST00000686842.1:n.7223T=
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ENST00000687279.1:c.3666T=
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ENSP00000508692.1:p.Leu1222=
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ENST00000687311.1:n.3632T=
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ENST00000687633.1:c.3570T=
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ENSP00000510289.1:p.Leu1190=
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ENST00000688923.1:n.3041T=
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ENST00000689688.1:c.3669T=
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ENSP00000510155.1:p.Leu1223=
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ENST00000690646.1:c.3573T=
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ENSP00000510383.1:p.Leu1191=
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ENST00000690814.1:c.*845T=
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ENSP00000508792.1:n.*845T=
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ENST00000691504.1:n.3563T=
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ENST00000692155.1:c.3749T=
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ENSP00000510290.1:n.3749T=
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ENST00000692746.1:n.3576T=
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ENST00000693386.1:c.3573T=
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ENSP00000510003.1:p.Leu1191=
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ENST00000693433.1:n.3563T=
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ENST00000693714.1:n.3616T=
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ENST00000693728.1:c.3573T=
|
ENSP00000510580.1:p.Leu1191=
|
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ENST00000349780.9:c.3669T=
MANE Select
|
ENSP00000343818.4:p.Leu1223=
|
|
|
ENST00000349780.8:c.3669T=
|
ENSP00000343818.4:p.Leu1223=
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ENST00000360190.8:c.3669T=
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ENSP00000353317.4:p.Leu1223=
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ENST00000360822.7:c.2979T=
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ENSP00000354065.4:p.Leu993=
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ENST00000416449.5:c.1851T=
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ENSP00000400395.1:p.Leu617=
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ENST00000425647.1:c.699T=
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ENSP00000409941.1:p.Leu233=
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ENST00000473282.6:c.*2493T=
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ENSP00000419265.1:n.*2493T=
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ENST00000480112.5:c.*1496T=
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ENSP00000418418.1:n.*1496T=
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ENST00000483412.5:n.2977T=
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NM_001011649.2:c.3669T=
|
NP_001011649.1:p.Leu1223=
|
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NM_001272039.1:c.2979T=
|
NP_001258968.1:p.Leu993=
|
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NM_018249.5:c.3669T=
|
NP_060719.4:p.Leu1223=
|
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NR_073554.1:n.3938T=
|
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NR_073555.1:n.3861T=
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NR_073556.1:n.4068T=
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NR_073557.1:n.3941T=
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NR_073558.1:n.3938T=
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XM_006717182.1:c.3573T=
|
XP_006717245.1:p.Leu1191=
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XM_006717185.1:c.2982T=
|
XP_006717248.1:p.Leu994=
|
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XM_011518860.1:c.3666T=
|
XP_011517162.1:p.Leu1222=
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XM_011518861.1:c.3666T=
|
XP_011517163.1:p.Leu1222=
|
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XM_017014921.1:c.3570T=
|
XP_016870410.1:p.Leu1190=
|
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XM_017014922.1:c.2835T=
|
XP_016870411.1:p.Leu945=
|
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XM_017014923.1:c.2982T=
|
XP_016870412.1:p.Leu994=
|
|
|
XM_017014924.1:c.1464T=
|
XP_016870413.1:p.Leu488=
|
|
|
NM_018249.6:c.3669T=
MANE Select
|
NP_060719.4:p.Leu1223=
|
|
|
NM_001011649.3:c.3669T=
|
NP_001011649.1:p.Leu1223=
|
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NR_073554.2:n.3935T=
|
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NR_073555.2:n.3858T=
|
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NR_073556.2:n.4065T=
|
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NR_073557.2:n.3938T=
|
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NR_073558.2:n.3935T=
|
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|
NM_001272039.2:c.2979T=
|
NP_001258968.1:p.Leu993=
|
|
