ENST00000359478.7:c.12G>C
MANE Select
|
ENSP00000352455.2:p.Leu4Phe
|
|
ENST00000359478.6:c.12G>C
|
ENSP00000352455.2:p.Leu4Phe
|
|
ENST00000396549.6:c.12G>C
|
ENSP00000379798.2:p.Leu4Phe
|
|
ENST00000433590.6:c.12G>C
|
ENSP00000411997.2:p.Leu4Phe
|
|
ENST00000534833.5:n.63G>C
|
|
|
ENST00000535336.5:c.12G>C
|
ENSP00000438525.1:p.Leu4Phe
|
|
ENST00000537009.5:c.12G>C
|
ENSP00000439289.1:p.Leu4Phe
|
|
ENST00000537128.1:n.276G>C
|
|
|
ENST00000538107.5:n.276G>C
|
|
|
ENST00000540087.5:c.12G>C
|
ENSP00000440496.1:p.Leu4Phe
|
|
ENST00000543369.5:c.12G>C
|
ENSP00000441492.1:p.Leu4Phe
|
|
ENST00000544211.5:c.12G>C
|
ENSP00000443839.1:p.Leu4Phe
|
|
ENST00000544889.1:c.12G>C
|
ENSP00000445799.1:p.Leu4Phe
|
|
NM_001297709.1:c.12G>C
|
NP_001284638.1:p.Leu4Phe
|
|
NM_001297710.1:c.12G>C
|
NP_001284639.1:p.Leu4Phe
|
|
NM_001297711.1:c.12G>C
|
NP_001284640.1:p.Leu4Phe
|
|
NM_001297712.1:c.12G>C
|
NP_001284641.1:p.Leu4Phe
|
|
NM_003480.3:c.12G>C
|
NP_003471.1:p.Leu4Phe
|
|
NR_123733.1:n.276G>C
|
|
|
NR_123734.1:n.276G>C
|
|
|
NM_003480.4:c.12G>C
MANE Select
|
NP_003471.1:p.Leu4Phe
|
|
NM_001297709.2:c.12G>C
|
NP_001284638.1:p.Leu4Phe
|
|
NM_001297710.2:c.12G>C
|
NP_001284639.1:p.Leu4Phe
|
|
NM_001297711.2:c.12G>C
|
NP_001284640.1:p.Leu4Phe
|
|
NM_001297712.2:c.12G>C
|
NP_001284641.1:p.Leu4Phe
|
|
NR_123733.2:n.214G>C
|
|
|
NR_123734.2:n.214G>C
|
|
|