|
ENST00000647720.2:c.3320T>C
|
ENSP00000497673.2:p.Phe1107Ser
|
|
|
ENST00000647978.2:c.*3034T>C
|
ENSP00000497658.1:n.*3034T>C
|
|
|
ENST00000649781.2:c.3137T>C
|
ENSP00000497203.1:p.Phe1046Ser
|
|
|
ENST00000685018.2:c.3320T>C
|
ENSP00000510194.2:p.Phe1107Ser
|
|
|
ENST00000687278.2:c.3320T>C
|
ENSP00000509593.2:p.Phe1107Ser
|
|
|
ENST00000699585.1:c.3320T>C
|
ENSP00000514456.1:p.Phe1107Ser
|
|
|
ENST00000699598.1:c.3320T>C
|
ENSP00000514467.1:p.Phe1107Ser
|
|
|
ENST00000699599.1:c.3320T>C
|
ENSP00000514468.1:p.Phe1107Ser
|
|
|
ENST00000699600.1:c.3320T>C
|
ENSP00000514469.1:p.Phe1107Ser
|
|
|
ENST00000699601.1:c.*1620T>C
|
ENSP00000514470.1:n.*1620T>C
|
|
|
ENST00000699602.1:c.3320T>C
|
ENSP00000514471.1:p.Phe1107Ser
|
|
|
ENST00000699604.1:c.*3144T>C
|
ENSP00000514472.1:n.*3144T>C
|
|
|
ENST00000699605.1:c.2894T>C
|
ENSP00000514473.1:p.Phe965Ser
|
|
|
ENST00000685018.1:c.68T>C
|
ENSP00000510194.1:p.Phe23Ser
|
|
|
ENST00000687278.1:c.911T>C
|
ENSP00000509593.1:p.Phe304Ser
|
|
|
ENST00000003084.11:c.3320T>C
MANE Select
|
ENSP00000003084.6:p.Phe1107Ser
|
|
|
ENST00000647720.1:c.970T>C
|
|
|
|
ENST00000648260.1:c.2102T>C
|
ENSP00000497957.1:p.Phe701Ser
|
|
|
ENST00000649406.1:c.3137T>C
|
ENSP00000497965.1:p.Phe1046Ser
|
|
|
ENST00000649781.1:c.3137T>C
|
ENSP00000497203.1:p.Phe1046Ser
|
|
|
ENST00000003084.10:c.3320T>C
|
ENSP00000003084.6:p.Phe1107Ser
|
|
|
ENST00000426809.5:c.3230T>C
|
ENSP00000389119.1:p.Phe1077Ser
|
|
|
ENST00000468795.1:c.145T>C
|
|
|
|
NM_000492.3:c.3320T>C , LRG_663t1:c.3320T>C
|
NP_000483.3:p.Phe1107Ser
|
|
|
XM_011515751.1:c.3410T>C
|
XP_011514053.1:p.Phe1137Ser
|
|
|
XM_011515752.1:c.3410T>C
|
XP_011514054.1:p.Phe1137Ser
|
|
|
XM_011515753.1:c.3077T>C
|
XP_011514055.1:p.Phe1026Ser
|
|
|
XM_011515754.1:c.3077T>C
|
XP_011514056.1:p.Phe1026Ser
|
|
|
NM_000492.4:c.3320T>C
MANE Select
|
NP_000483.3:p.Phe1107Ser
|
|
