ENST00000389048.8:c.3609C>T
MANE Select
|
ENSP00000373700.3:p.Asp1203=
|
|
ENST00000431873.6:c.836C>T
|
|
|
ENST00000638605.1:n.486C>T
|
|
|
ENST00000642122.1:c.405C>T
|
ENSP00000493203.1:p.Asp135=
|
|
ENST00000389048.7:c.3609C>T
|
ENSP00000373700.3:p.Asp1203=
|
|
ENST00000431873.5:c.489C>T
|
ENSP00000414027.2:p.Asp163=
|
|
ENST00000618119.4:c.2478C>T
|
ENSP00000482733.1:p.Asp826=
|
|
NM_004304.4:c.3609C>T
|
NP_004295.2:p.Asp1203=
|
|
NM_001353765.1:c.405C>T
|
NP_001340694.1:p.Asp135=
|
|
XM_024452778.1:c.762C>T
|
XP_024308546.1:p.Asp254=
|
|
XM_024452779.1:c.405C>T
|
XP_024308547.1:p.Asp135=
|
|
NM_004304.5:c.3609C>T
MANE Select
|
NP_004295.2:p.Asp1203=
|
|
NM_001353765.2:c.405C>T
|
NP_001340694.1:p.Asp135=
|
|