ENST00000647720.2:c.3575A>T
|
ENSP00000497673.2:p.Glu1192Val
|
|
ENST00000647978.2:c.*3489A>T
|
ENSP00000497658.1:n.*3489A>T
|
|
ENST00000649781.2:c.3592A>T
|
ENSP00000497203.1:p.Arg1198Ter
|
|
ENST00000685018.2:c.3775A>T
|
ENSP00000510194.2:p.Arg1259Ter
|
|
ENST00000687278.2:c.*428A>T
|
ENSP00000509593.2:n.*428A>T
|
|
ENST00000699585.1:c.3575A>T
|
ENSP00000514456.1:p.Glu1192Val
|
|
ENST00000699598.1:c.3775A>T
|
ENSP00000514467.1:p.Arg1259Ter
|
|
ENST00000699599.1:c.3775A>T
|
ENSP00000514468.1:p.Arg1259Ter
|
|
ENST00000699600.1:c.*436A>T
|
ENSP00000514469.1:n.*436A>T
|
|
ENST00000699601.1:c.*2150A>T
|
ENSP00000514470.1:n.*2150A>T
|
|
ENST00000699602.1:c.3769A>T
|
ENSP00000514471.1:p.Arg1257Ter
|
|
ENST00000699604.1:c.*3599A>T
|
ENSP00000514472.1:n.*3599A>T
|
|
ENST00000699605.1:c.3349A>T
|
ENSP00000514473.1:p.Arg1117Ter
|
|
ENST00000685018.1:c.523A>T
|
ENSP00000510194.1:p.Arg175Ter
|
|
ENST00000687278.1:c.1562A>T
|
ENSP00000509593.1:n.1562A>T
|
|
ENST00000689011.1:c.357A>T
|
|
|
ENST00000003084.11:c.3775A>T
MANE Select
|
ENSP00000003084.6:p.Arg1259Ter
|
|
ENST00000647720.1:c.1225A>T
|
|
|
ENST00000649781.1:c.3592A>T
|
ENSP00000497203.1:p.Arg1198Ter
|
|
ENST00000003084.10:c.3775A>T
|
ENSP00000003084.6:p.Arg1259Ter
|
|
ENST00000426809.5:c.3685A>T
|
ENSP00000389119.1:p.Arg1229Ter
|
|
NM_000492.3:c.3775A>T , LRG_663t1:c.3775A>T
|
NP_000483.3:p.Arg1259Ter
|
|
XM_011515751.1:c.3865A>T
|
XP_011514053.1:p.Arg1289Ter
|
|
XM_011515752.1:c.3865A>T
|
XP_011514054.1:p.Arg1289Ter
|
|
XM_011515753.1:c.3532A>T
|
XP_011514055.1:p.Arg1178Ter
|
|
XM_011515754.1:c.3532A>T
|
XP_011514056.1:p.Arg1178Ter
|
|
NM_000492.4:c.3775A>T
MANE Select
|
NP_000483.3:p.Arg1259Ter
|
|