ENST00000216927.4:c.785C>T
|
ENSP00000216927.4:p.Ala262Val
|
|
ENST00000303415.7:c.1118C>T
MANE Select
|
ENSP00000305529.3:p.Ala373Val
|
|
ENST00000344103.8:c.467C>T
|
ENSP00000342759.4:p.Ala156Val
|
|
ENST00000381580.5:c.1019C>T
|
ENSP00000370992.1:p.Ala340Val
|
|
ENST00000381583.6:c.785C>T
|
ENSP00000370995.2:p.Ala262Val
|
|
ENST00000478145.6:n.179C>T
|
|
|
ENST00000497407.2:n.267C>T
|
|
|
NM_001039508.1:c.785C>T
|
NP_001034597.1:p.Ala262Val
|
|
NM_018556.3:c.1118C>T
|
NP_061026.2:p.Ala373Val
|
|
NM_080816.2:c.467C>T
|
NP_543006.2:p.Ala156Val
|
|
XM_005260749.2:c.800C>T
|
XP_005260806.1:p.Ala267Val
|
|
XM_011529286.1:c.1019C>T
|
XP_011527588.1:p.Ala340Val
|
|
XM_005260749.4:c.800C>T
|
XP_005260806.1:p.Ala267Val
|
|
XM_011529286.2:c.1019C>T
|
XP_011527588.1:p.Ala340Val
|
|
NM_018556.4:c.1118C>T
MANE Select
|
NP_061026.2:p.Ala373Val
|
|
NM_080816.3:c.467C>T
|
NP_543006.2:p.Ala156Val
|
|
NM_001039508.2:c.785C>T
|
NP_001034597.1:p.Ala262Val
|
|