ENST00000399408.7:c.507G>A
|
ENSP00000382340.4:p.Leu169=
|
|
ENST00000399410.8:c.507G>A
MANE Select
|
ENSP00000382342.3:p.Leu169=
|
|
ENST00000572882.3:c.507G>A
|
ENSP00000461615.2:p.Leu169=
|
|
ENST00000574224.2:n.582G>A
|
|
|
ENST00000677164.1:c.489+1885G>A
|
ENSP00000502873.1:n.489+1885G>A
|
|
ENST00000678422.1:c.507G>A
|
ENSP00000503954.1:p.Leu169=
|
|
ENST00000679043.1:n.459G>A
|
|
|
ENST00000399408.6:c.-472G>A
|
ENSP00000382340.3:n.-472G>A
|
|
ENST00000399410.7:c.507G>A
|
ENSP00000382342.3:p.Leu169=
|
|
ENST00000572882.2:c.202G>A
|
|
|
ENST00000574224.1:n.107G>A
|
|
|
NM_004996.3:c.507G>A
|
NP_004987.2:p.Leu169=
|
|
XM_011522497.1:c.483G>A
|
XP_011520799.1:p.Leu161=
|
|
XM_011522498.1:c.561G>A
|
XP_011520800.1:p.Leu187=
|
|
XM_011522498.2:c.561G>A
|
XP_011520800.1:p.Leu187=
|
|
XM_017023237.1:c.561G>A
|
XP_016878726.1:p.Leu187=
|
|
XM_017023238.1:c.543+1885G>A
|
XP_016878727.1:n.543+1885G>A
|
|
XM_017023239.1:c.423G>A
|
XP_016878728.1:p.Leu141=
|
|
XM_017023240.1:c.561G>A
|
XP_016878729.1:p.Leu187=
|
|
XM_017023241.1:c.405+6612G>A
|
XP_016878730.1:n.405+6612G>A
|
|
XM_017023242.1:c.561G>A
|
XP_016878731.1:p.Leu187=
|
|
XM_017023243.2:c.561G>A
|
XP_016878732.1:p.Leu187=
|
|
NM_004996.4:c.507G>A
MANE Select
|
NP_004987.2:p.Leu169=
|
|