ENST00000525341.2:c.1153G>C
|
|
|
ENST00000528641.7:c.657G>C
|
ENSP00000434982.3:p.Gln219His
|
|
ENST00000529797.2:n.1688G>C
|
|
|
ENST00000682324.1:c.469-151G>C
|
ENSP00000508017.1:n.469-151G>C
|
|
ENST00000682659.1:c.477G>C
|
ENSP00000507351.1:p.Gln159His
|
|
ENST00000682699.1:c.846G>C
|
ENSP00000507935.1:p.Gln282His
|
|
ENST00000683237.1:c.838G>C
|
ENSP00000507343.1:p.Gly280Arg
|
|
ENST00000683856.1:c.669G>C
|
ENSP00000507979.1:p.Gln223His
|
|
ENST00000684006.1:c.835G>C
|
ENSP00000507269.1:p.Gly279Arg
|
|
ENST00000684657.1:c.666G>C
|
ENSP00000507961.1:p.Gln222His
|
|
ENST00000279146.8:c.846G>C
MANE Select
|
ENSP00000279146.3:p.Gln282His
|
|
ENST00000279146.7:c.846G>C
|
ENSP00000279146.3:p.Gln282His
|
|
ENST00000528641.6:c.657G>C
|
ENSP00000434982.2:p.Gln219His
|
|
NM_001302959.1:c.669G>C
|
NP_001289888.1:p.Gln223His
|
|
NM_001302960.1:c.838G>C
|
NP_001289889.1:p.Gly280Arg
|
|
NM_003977.3:c.846G>C
|
NP_003968.3:p.Gln282His
|
|
XM_024448761.1:c.846G>C
|
XP_024304529.1:p.Gln282His
|
|
NM_003977.4:c.846G>C
MANE Select
|
NP_003968.3:p.Gln282His
|
|
NM_001302960.2:c.838G>C
|
NP_001289889.1:p.Gly280Arg
|
|
NM_001302959.2:c.669G>C
|
NP_001289888.1:p.Gln223His
|
|