ENST00000216927.4:c.790C>T
|
ENSP00000216927.4:p.Leu264Phe
|
|
ENST00000303415.7:c.1123C>T
MANE Select
|
ENSP00000305529.3:p.Leu375Phe
|
|
ENST00000344103.8:c.472C>T
|
ENSP00000342759.4:p.Leu158Phe
|
|
ENST00000381580.5:c.1024C>T
|
ENSP00000370992.1:p.Leu342Phe
|
|
ENST00000381583.6:c.790C>T
|
ENSP00000370995.2:p.Leu264Phe
|
|
ENST00000478145.6:n.184C>T
|
|
|
ENST00000497407.2:n.272C>T
|
|
|
NM_001039508.1:c.790C>T
|
NP_001034597.1:p.Leu264Phe
|
|
NM_018556.3:c.1123C>T
|
NP_061026.2:p.Leu375Phe
|
|
NM_080816.2:c.472C>T
|
NP_543006.2:p.Leu158Phe
|
|
XM_005260749.2:c.805C>T
|
XP_005260806.1:p.Leu269Phe
|
|
XM_011529286.1:c.1024C>T
|
XP_011527588.1:p.Leu342Phe
|
|
XM_005260749.4:c.805C>T
|
XP_005260806.1:p.Leu269Phe
|
|
XM_011529286.2:c.1024C>T
|
XP_011527588.1:p.Leu342Phe
|
|
NM_018556.4:c.1123C>T
MANE Select
|
NP_061026.2:p.Leu375Phe
|
|
NM_080816.3:c.472C>T
|
NP_543006.2:p.Leu158Phe
|
|
NM_001039508.2:c.790C>T
|
NP_001034597.1:p.Leu264Phe
|
|