ENST00000449291.7:c.1277T>A
MANE Select
|
ENSP00000401508.2:p.Leu426His
|
|
ENST00000340490.7:c.1277T>A
|
ENSP00000341136.3:p.Leu426His
|
|
ENST00000426292.7:c.1277T>A
|
ENSP00000390949.3:p.Leu426His
|
|
ENST00000435154.7:c.1277T>A
|
ENSP00000405670.3:p.Leu426His
|
|
ENST00000449291.6:c.1277T>A
|
ENSP00000401508.2:p.Leu426His
|
|
ENST00000460623.5:c.255T>A
|
|
|
ENST00000464332.5:n.821T>A
|
|
|
ENST00000525583.5:c.1061T>A
|
|
|
NM_001286829.1:c.1277T>A
|
NP_001273758.1:p.Leu426His
|
|
NM_145201.5:c.1277T>A
|
NP_660202.3:p.Leu426His
|
|
XM_011517377.1:c.1277T>A
|
XP_011515679.1:p.Leu426His
|
|
NM_001363145.1:c.1196T>A
|
NP_001350074.1:p.Leu399His
|
|
NM_001363146.1:c.593T>A
|
NP_001350075.1:p.Leu198His
|
|
XM_017013975.2:c.1496T>A
|
XP_016869464.1:p.Leu499His
|
|
XM_017013976.2:c.1496T>A
|
XP_016869465.1:p.Leu499His
|
|
XM_017013977.2:c.1196T>A
|
XP_016869466.1:p.Leu399His
|
|
XM_017013978.2:c.1496T>A
|
XP_016869467.1:p.Leu499His
|
|
XM_017013979.2:c.593T>A
|
XP_016869468.1:p.Leu198His
|
|
XM_024447332.1:c.914T>A
|
XP_024303100.1:p.Leu305His
|
|
XM_024447333.1:c.512T>A
|
XP_024303101.1:p.Leu171His
|
|
NM_145201.6:c.1277T>A
MANE Select
|
NP_660202.3:p.Leu426His
|
|
NM_001286829.2:c.1277T>A
|
NP_001273758.1:p.Leu426His
|
|