ENST00000389048.8:c.3472G>T
MANE Select
|
ENSP00000373700.3:p.Glu1158Ter
|
|
ENST00000431873.6:c.699G>T
|
|
|
ENST00000638605.1:n.349G>T
|
|
|
ENST00000642122.1:c.268G>T
|
ENSP00000493203.1:p.Glu90Ter
|
|
ENST00000389048.7:c.3472G>T
|
ENSP00000373700.3:p.Glu1158Ter
|
|
ENST00000431873.5:c.352G>T
|
ENSP00000414027.2:p.Glu118Ter
|
|
ENST00000453137.1:c.166G>T
|
ENSP00000387488.1:p.Glu56Ter
|
|
ENST00000618119.4:c.2341G>T
|
ENSP00000482733.1:p.Glu781Ter
|
|
NM_004304.4:c.3472G>T
|
NP_004295.2:p.Glu1158Ter
|
|
NM_001353765.1:c.268G>T
|
NP_001340694.1:p.Glu90Ter
|
|
XM_024452778.1:c.625G>T
|
XP_024308546.1:p.Glu209Ter
|
|
XM_024452779.1:c.268G>T
|
XP_024308547.1:p.Glu90Ter
|
|
NM_004304.5:c.3472G>T
MANE Select
|
NP_004295.2:p.Glu1158Ter
|
|
NM_001353765.2:c.268G>T
|
NP_001340694.1:p.Glu90Ter
|
|