ENST00000700367.1:c.319-143G>T
|
ENSP00000514965.1:n.319-143G>T
|
|
ENST00000354546.10:c.319-143G>T
MANE Select
|
ENSP00000346550.5:n.319-143G>T
|
|
ENST00000354546.9:c.319-143G>T
|
ENSP00000346550.5:n.319-143G>T
|
|
ENST00000377751.9:c.204+1889G>T
|
ENSP00000366980.5:n.204+1889G>T
|
|
ENST00000517486.5:c.318+1214G>T
|
ENSP00000428916.1:n.318+1214G>T
|
|
ENST00000517677.5:c.319-143G>T
|
ENSP00000430826.1:n.319-143G>T
|
|
ENST00000517757.5:c.223-143G>T
|
ENSP00000430572.1:n.223-143G>T
|
|
ENST00000519644.6:c.262+1270G>T
|
ENSP00000430663.2:n.262+1270G>T
|
|
ENST00000520378.1:n.1011-143G>T
|
|
|
ENST00000521512.5:c.224+1308G>T
|
ENSP00000430420.1:n.224+1308G>T
|
|
ENST00000521749.5:c.223-143G>T
|
ENSP00000430429.1:n.223-143G>T
|
|
ENST00000523164.1:c.319-143G>T
|
ENSP00000431078.1:n.319-143G>T
|
|
ENST00000523714.5:c.223-143G>T
|
ENSP00000430517.1:n.223-143G>T
|
|
NM_001155.4:c.319-143G>T
|
NP_001146.2:n.319-143G>T
|
|
NM_001193544.1:c.223-143G>T
|
NP_001180473.1:n.223-143G>T
|
|
XM_005268432.3:c.319-143G>T
|
XP_005268489.1:n.319-143G>T
|
|
NM_001363114.1:c.319-143G>T
|
NP_001350043.1:n.319-143G>T
|
|
NM_001155.5:c.319-143G>T
MANE Select
|
NP_001146.2:n.319-143G>T
|
|
NM_001193544.2:c.223-143G>T
|
NP_001180473.1:n.223-143G>T
|
|
NM_001363114.2:c.319-143G>T
|
NP_001350043.1:n.319-143G>T
|
|