ENST00000525341.2:c.761G>C
|
|
|
ENST00000528641.7:c.595G>C
|
ENSP00000434982.3:p.Asp199His
|
|
ENST00000529797.2:n.1296G>C
|
|
|
ENST00000682324.1:c.469-543G>C
|
ENSP00000508017.1:n.469-543G>C
|
|
ENST00000682659.1:c.415G>C
|
ENSP00000507351.1:p.Asp139His
|
|
ENST00000682699.1:c.784G>C
|
ENSP00000507935.1:p.Asp262His
|
|
ENST00000683237.1:c.779+5G>C
|
ENSP00000507343.1:n.779+5G>C
|
|
ENST00000683856.1:c.607G>C
|
ENSP00000507979.1:p.Asp203His
|
|
ENST00000684006.1:c.784G>C
|
ENSP00000507269.1:p.Asp262His
|
|
ENST00000684657.1:c.604G>C
|
ENSP00000507961.1:p.Asp202His
|
|
ENST00000279146.8:c.784G>C
MANE Select
|
ENSP00000279146.3:p.Asp262His
|
|
ENST00000279146.7:c.784G>C
|
ENSP00000279146.3:p.Asp262His
|
|
ENST00000525341.1:c.436G>C
|
ENSP00000476993.1:p.Asp146His
|
|
ENST00000528641.6:c.595G>C
|
ENSP00000434982.2:p.Asp199His
|
|
NM_001302959.1:c.607G>C
|
NP_001289888.1:p.Asp203His
|
|
NM_001302960.1:c.779+5G>C
|
NP_001289889.1:n.779+5G>C
|
|
NM_003977.3:c.784G>C
|
NP_003968.3:p.Asp262His
|
|
XM_024448761.1:c.784G>C
|
XP_024304529.1:p.Asp262His
|
|
NM_003977.4:c.784G>C
MANE Select
|
NP_003968.3:p.Asp262His
|
|
NM_001302960.2:c.779+5G>C
|
NP_001289889.1:n.779+5G>C
|
|
NM_001302959.2:c.607G>C
|
NP_001289888.1:p.Asp203His
|
|