|
ENST00000647720.2:c.3487G>T
|
ENSP00000497673.2:p.Val1163Phe
|
|
|
ENST00000647978.2:c.*3201G>T
|
ENSP00000497658.1:n.*3201G>T
|
|
|
ENST00000649781.2:c.3304G>T
|
ENSP00000497203.1:p.Val1102Phe
|
|
|
ENST00000685018.2:c.3487G>T
|
ENSP00000510194.2:p.Val1163Phe
|
|
|
ENST00000687278.2:c.*140G>T
|
ENSP00000509593.2:n.*140G>T
|
|
|
ENST00000699585.1:c.3487G>T
|
ENSP00000514456.1:p.Val1163Phe
|
|
|
ENST00000699598.1:c.3487G>T
|
ENSP00000514467.1:p.Val1163Phe
|
|
|
ENST00000699599.1:c.3487G>T
|
ENSP00000514468.1:p.Val1163Phe
|
|
|
ENST00000699600.1:c.*148G>T
|
ENSP00000514469.1:n.*148G>T
|
|
|
ENST00000699601.1:c.*1862G>T
|
ENSP00000514470.1:n.*1862G>T
|
|
|
ENST00000699602.1:c.3481G>T
|
ENSP00000514471.1:p.Val1161Phe
|
|
|
ENST00000699604.1:c.*3311G>T
|
ENSP00000514472.1:n.*3311G>T
|
|
|
ENST00000699605.1:c.3061G>T
|
ENSP00000514473.1:p.Val1021Phe
|
|
|
ENST00000685018.1:c.235G>T
|
ENSP00000510194.1:p.Val79Phe
|
|
|
ENST00000687278.1:c.1274G>T
|
ENSP00000509593.1:n.1274G>T
|
|
|
ENST00000689011.1:c.69G>T
|
|
|
|
ENST00000003084.11:c.3487G>T
MANE Select
|
ENSP00000003084.6:p.Val1163Phe
|
|
|
ENST00000647720.1:c.1137G>T
|
|
|
|
ENST00000648260.1:c.2269G>T
|
ENSP00000497957.1:p.Val757Phe
|
|
|
ENST00000649406.1:c.3304G>T
|
ENSP00000497965.1:p.Val1102Phe
|
|
|
ENST00000649781.1:c.3304G>T
|
ENSP00000497203.1:p.Val1102Phe
|
|
|
ENST00000003084.10:c.3487G>T
|
ENSP00000003084.6:p.Val1163Phe
|
|
|
ENST00000426809.5:c.3397G>T
|
ENSP00000389119.1:p.Val1133Phe
|
|
|
ENST00000468795.1:c.312G>T
|
|
|
|
NM_000492.3:c.3487G>T , LRG_663t1:c.3487G>T
|
NP_000483.3:p.Val1163Phe
|
|
|
XM_011515751.1:c.3577G>T
|
XP_011514053.1:p.Val1193Phe
|
|
|
XM_011515752.1:c.3577G>T
|
XP_011514054.1:p.Val1193Phe
|
|
|
XM_011515753.1:c.3244G>T
|
XP_011514055.1:p.Val1082Phe
|
|
|
XM_011515754.1:c.3244G>T
|
XP_011514056.1:p.Val1082Phe
|
|
|
NM_000492.4:c.3487G>T
MANE Select
|
NP_000483.3:p.Val1163Phe
|
|
