ENST00000433363.7:c.987G>C
MANE Select
|
ENSP00000406220.2:p.Leu329=
|
|
ENST00000293800.10:c.936G>C
|
ENSP00000293800.6:p.Leu312=
|
|
ENST00000381074.8:c.858G>C
|
ENSP00000370464.4:p.Leu286=
|
|
ENST00000433363.6:c.987G>C
|
ENSP00000406220.2:p.Leu329=
|
|
ENST00000572727.1:n.96G>C
|
|
|
ENST00000573648.5:c.987G>C
|
ENSP00000459372.1:p.Leu329=
|
|
ENST00000574824.5:n.2120G>C
|
|
|
NM_001143838.2:c.987G>C
|
NP_001137310.1:p.Leu329=
|
|
NM_001284509.1:c.936G>C
|
NP_001271438.1:p.Leu312=
|
|
NM_001284510.1:c.858G>C
|
NP_001271439.1:p.Leu286=
|
|
NM_177550.4:c.987G>C , LRG_1020t1:c.987G>C
|
NP_808218.1:p.Leu329=
|
|
XM_006721504.2:c.876G>C
|
XP_006721567.1:p.Leu292=
|
|
XM_011523795.1:c.987G>C
|
XP_011522097.1:p.Leu329=
|
|
XM_011523795.3:c.987G>C
|
XP_011522097.1:p.Leu329=
|
|
NM_001143838.3:c.987G>C
|
NP_001137310.1:p.Leu329=
|
|
NM_001284509.2:c.936G>C
|
NP_001271438.1:p.Leu312=
|
|
NM_001284510.2:c.858G>C
|
NP_001271439.1:p.Leu286=
|
|
NM_177550.5:c.987G>C
MANE Select
|
NP_808218.1:p.Leu329=
|
|