ENST00000525341.2:c.955G>T
|
|
|
ENST00000528641.7:c.599-140G>T
|
ENSP00000434982.3:n.599-140G>T
|
|
ENST00000529797.2:n.1490G>T
|
|
|
ENST00000682324.1:c.469-349G>T
|
ENSP00000508017.1:n.469-349G>T
|
|
ENST00000682659.1:c.419-140G>T
|
ENSP00000507351.1:n.419-140G>T
|
|
ENST00000682699.1:c.788-140G>T
|
ENSP00000507935.1:n.788-140G>T
|
|
ENST00000683237.1:c.780-140G>T
|
ENSP00000507343.1:n.780-140G>T
|
|
ENST00000683856.1:c.611-140G>T
|
ENSP00000507979.1:n.611-140G>T
|
|
ENST00000684006.1:c.788-151G>T
|
ENSP00000507269.1:n.788-151G>T
|
|
ENST00000684657.1:c.608-140G>T
|
ENSP00000507961.1:n.608-140G>T
|
|
ENST00000279146.8:c.788-140G>T
MANE Select
|
ENSP00000279146.3:n.788-140G>T
|
|
ENST00000279146.7:c.788-140G>T
|
ENSP00000279146.3:n.788-140G>T
|
|
ENST00000525341.1:c.630G>T
|
ENSP00000476993.1:n.630G>T
|
|
ENST00000528641.6:c.599-140G>T
|
ENSP00000434982.2:n.599-140G>T
|
|
NM_001302959.1:c.611-140G>T
|
NP_001289888.1:n.611-140G>T
|
|
NM_001302960.1:c.780-140G>T
|
NP_001289889.1:n.780-140G>T
|
|
NM_003977.3:c.788-140G>T
|
NP_003968.3:n.788-140G>T
|
|
XM_024448761.1:c.788-140G>T
|
XP_024304529.1:n.788-140G>T
|
|
NM_003977.4:c.788-140G>T
MANE Select
|
NP_003968.3:n.788-140G>T
|
|
NM_001302960.2:c.780-140G>T
|
NP_001289889.1:n.780-140G>T
|
|
NM_001302959.2:c.611-140G>T
|
NP_001289888.1:n.611-140G>T
|
|