ENST00000216927.4:c.756A>T
|
ENSP00000216927.4:p.Ala252=
|
|
ENST00000303415.7:c.1089A>T
MANE Select
|
ENSP00000305529.3:p.Ala363=
|
|
ENST00000344103.8:c.438A>T
|
ENSP00000342759.4:p.Ala146=
|
|
ENST00000381580.5:c.990A>T
|
ENSP00000370992.1:p.Ala330=
|
|
ENST00000381583.6:c.756A>T
|
ENSP00000370995.2:p.Ala252=
|
|
ENST00000478145.6:n.150A>T
|
|
|
ENST00000497407.2:n.238A>T
|
|
|
NM_001039508.1:c.756A>T
|
NP_001034597.1:p.Ala252=
|
|
NM_018556.3:c.1089A>T
|
NP_061026.2:p.Ala363=
|
|
NM_080816.2:c.438A>T
|
NP_543006.2:p.Ala146=
|
|
XM_005260749.2:c.771A>T
|
XP_005260806.1:p.Ala257=
|
|
XM_011529286.1:c.990A>T
|
XP_011527588.1:p.Ala330=
|
|
XM_005260749.4:c.771A>T
|
XP_005260806.1:p.Ala257=
|
|
XM_011529286.2:c.990A>T
|
XP_011527588.1:p.Ala330=
|
|
NM_018556.4:c.1089A>T
MANE Select
|
NP_061026.2:p.Ala363=
|
|
NM_080816.3:c.438A>T
|
NP_543006.2:p.Ala146=
|
|
NM_001039508.2:c.756A>T
|
NP_001034597.1:p.Ala252=
|
|