ENST00000647720.2:c.3577A>C
|
ENSP00000497673.2:p.Thr1193Pro
|
|
ENST00000647978.2:c.*3491A>C
|
ENSP00000497658.1:n.*3491A>C
|
|
ENST00000649781.2:c.3594A>C
|
ENSP00000497203.1:p.Arg1198Ser
|
|
ENST00000685018.2:c.3777A>C
|
ENSP00000510194.2:p.Arg1259Ser
|
|
ENST00000687278.2:c.*430A>C
|
ENSP00000509593.2:n.*430A>C
|
|
ENST00000699585.1:c.3577A>C
|
ENSP00000514456.1:p.Thr1193Pro
|
|
ENST00000699598.1:c.3777A>C
|
ENSP00000514467.1:p.Arg1259Ser
|
|
ENST00000699599.1:c.3777A>C
|
ENSP00000514468.1:p.Arg1259Ser
|
|
ENST00000699600.1:c.*438A>C
|
ENSP00000514469.1:n.*438A>C
|
|
ENST00000699601.1:c.*2152A>C
|
ENSP00000514470.1:n.*2152A>C
|
|
ENST00000699602.1:c.3771A>C
|
ENSP00000514471.1:p.Arg1257Ser
|
|
ENST00000699604.1:c.*3601A>C
|
ENSP00000514472.1:n.*3601A>C
|
|
ENST00000699605.1:c.3351A>C
|
ENSP00000514473.1:p.Arg1117Ser
|
|
ENST00000685018.1:c.525A>C
|
ENSP00000510194.1:p.Arg175Ser
|
|
ENST00000687278.1:c.1564A>C
|
ENSP00000509593.1:n.1564A>C
|
|
ENST00000689011.1:c.359A>C
|
|
|
ENST00000003084.11:c.3777A>C
MANE Select
|
ENSP00000003084.6:p.Arg1259Ser
|
|
ENST00000647720.1:c.1227A>C
|
|
|
ENST00000649781.1:c.3594A>C
|
ENSP00000497203.1:p.Arg1198Ser
|
|
ENST00000003084.10:c.3777A>C
|
ENSP00000003084.6:p.Arg1259Ser
|
|
ENST00000426809.5:c.3687A>C
|
ENSP00000389119.1:p.Arg1229Ser
|
|
NM_000492.3:c.3777A>C , LRG_663t1:c.3777A>C
|
NP_000483.3:p.Arg1259Ser
|
|
XM_011515751.1:c.3867A>C
|
XP_011514053.1:p.Arg1289Ser
|
|
XM_011515752.1:c.3867A>C
|
XP_011514054.1:p.Arg1289Ser
|
|
XM_011515753.1:c.3534A>C
|
XP_011514055.1:p.Arg1178Ser
|
|
XM_011515754.1:c.3534A>C
|
XP_011514056.1:p.Arg1178Ser
|
|
NM_000492.4:c.3777A>C
MANE Select
|
NP_000483.3:p.Arg1259Ser
|
|