ENST00000525341.2:c.951T>C
|
|
|
ENST00000528641.7:c.599-144T>C
|
ENSP00000434982.3:n.599-144T>C
|
|
ENST00000529797.2:n.1486T>C
|
|
|
ENST00000682324.1:c.469-353T>C
|
ENSP00000508017.1:n.469-353T>C
|
|
ENST00000682659.1:c.419-144T>C
|
ENSP00000507351.1:n.419-144T>C
|
|
ENST00000682699.1:c.788-144T>C
|
ENSP00000507935.1:n.788-144T>C
|
|
ENST00000683237.1:c.780-144T>C
|
ENSP00000507343.1:n.780-144T>C
|
|
ENST00000683856.1:c.611-144T>C
|
ENSP00000507979.1:n.611-144T>C
|
|
ENST00000684006.1:c.788-155T>C
|
ENSP00000507269.1:n.788-155T>C
|
|
ENST00000684657.1:c.608-144T>C
|
ENSP00000507961.1:n.608-144T>C
|
|
ENST00000279146.8:c.788-144T>C
MANE Select
|
ENSP00000279146.3:n.788-144T>C
|
|
ENST00000279146.7:c.788-144T>C
|
ENSP00000279146.3:n.788-144T>C
|
|
ENST00000525341.1:c.626T>C
|
ENSP00000476993.1:n.626T>C
|
|
ENST00000528641.6:c.599-144T>C
|
ENSP00000434982.2:n.599-144T>C
|
|
NM_001302959.1:c.611-144T>C
|
NP_001289888.1:n.611-144T>C
|
|
NM_001302960.1:c.780-144T>C
|
NP_001289889.1:n.780-144T>C
|
|
NM_003977.3:c.788-144T>C
|
NP_003968.3:n.788-144T>C
|
|
XM_024448761.1:c.788-144T>C
|
XP_024304529.1:n.788-144T>C
|
|
NM_003977.4:c.788-144T>C
MANE Select
|
NP_003968.3:n.788-144T>C
|
|
NM_001302960.2:c.780-144T>C
|
NP_001289889.1:n.780-144T>C
|
|
NM_001302959.2:c.611-144T>C
|
NP_001289888.1:n.611-144T>C
|
|