ENST00000376573.9:c.1036+192G>T
MANE Select
|
ENSP00000365757.4:n.1036+192G>T
|
|
ENST00000323883.11:c.616+192G>T
|
ENSP00000326294.7:n.616+192G>T
|
|
ENST00000376573.8:c.1036+192G>T
|
ENSP00000365757.4:n.1036+192G>T
|
|
ENST00000545335.5:c.859+192G>T
|
ENSP00000442098.1:n.859+192G>T
|
|
NM_005028.4:c.1036+192G>T
|
NP_005019.2:n.1036+192G>T
|
|
XM_006717450.2:c.883+192G>T
|
XP_006717513.1:n.883+192G>T
|
|
XM_011519494.1:c.997+192G>T
|
XP_011517796.1:n.997+192G>T
|
|
XM_011519495.1:c.949+192G>T
|
XP_011517797.1:n.949+192G>T
|
|
XM_011519496.1:c.859+192G>T
|
XP_011517798.1:n.859+192G>T
|
|
NM_001330062.1:c.859+192G>T
|
NP_001316991.1:n.859+192G>T
|
|
XM_017016330.1:c.859+192G>T
|
XP_016871819.1:n.859+192G>T
|
|
XM_017016331.1:c.859+192G>T
|
XP_016871820.1:n.859+192G>T
|
|
XM_017016332.1:c.706+192G>T
|
XP_016871821.1:n.706+192G>T
|
|
NM_005028.5:c.1036+192G>T
MANE Select
|
NP_005019.2:n.1036+192G>T
|
|
NM_001330062.2:c.859+192G>T
|
NP_001316991.1:n.859+192G>T
|
|