ENST00000525341.2:c.664G>C
|
|
|
ENST00000528641.7:c.498G>C
|
ENSP00000434982.3:p.Gln166His
|
|
ENST00000529797.2:n.1199G>C
|
|
|
ENST00000682324.1:c.469-640G>C
|
ENSP00000508017.1:n.469-640G>C
|
|
ENST00000682659.1:c.318G>C
|
ENSP00000507351.1:p.Gln106His
|
|
ENST00000682699.1:c.687G>C
|
ENSP00000507935.1:p.Gln229His
|
|
ENST00000683237.1:c.687G>C
|
ENSP00000507343.1:p.Gln229His
|
|
ENST00000683856.1:c.510G>C
|
ENSP00000507979.1:p.Gln170His
|
|
ENST00000684006.1:c.687G>C
|
ENSP00000507269.1:p.Gln229His
|
|
ENST00000684657.1:c.507G>C
|
ENSP00000507961.1:p.Gln169His
|
|
ENST00000279146.8:c.687G>C
MANE Select
|
ENSP00000279146.3:p.Gln229His
|
|
ENST00000279146.7:c.687G>C
|
ENSP00000279146.3:p.Gln229His
|
|
ENST00000525341.1:c.339G>C
|
ENSP00000476993.1:p.Gln113His
|
|
ENST00000528641.6:c.498G>C
|
ENSP00000434982.2:p.Gln166His
|
|
NM_001302959.1:c.510G>C
|
NP_001289888.1:p.Gln170His
|
|
NM_001302960.1:c.687G>C
|
NP_001289889.1:p.Gln229His
|
|
NM_003977.3:c.687G>C
|
NP_003968.3:p.Gln229His
|
|
XM_024448761.1:c.687G>C
|
XP_024304529.1:p.Gln229His
|
|
NM_003977.4:c.687G>C
MANE Select
|
NP_003968.3:p.Gln229His
|
|
NM_001302960.2:c.687G>C
|
NP_001289889.1:p.Gln229His
|
|
NM_001302959.2:c.510G>C
|
NP_001289888.1:p.Gln170His
|
|