|
ENST00000310638.9:c.1223-259G>A
MANE Select
|
ENSP00000311095.4:n.1223-259G>A
|
|
|
ENST00000310638.8:c.1223-259G>A
|
ENSP00000311095.4:n.1223-259G>A
|
|
|
ENST00000371904.8:c.1226-259G>A
|
ENSP00000360971.4:n.1226-259G>A
|
|
|
ENST00000371905.1:c.1223-259G>A
|
ENSP00000360972.1:n.1223-259G>A
|
|
|
ENST00000462347.5:c.929-259G>A
|
ENSP00000477495.1:n.929-259G>A
|
|
|
ENST00000465874.5:c.*21-259G>A
|
ENSP00000476368.1:n.*21-259G>A
|
|
|
ENST00000468629.5:c.1127-469G>A
|
ENSP00000476619.1:n.1127-469G>A
|
|
|
ENST00000474458.5:c.743-469G>A
|
ENSP00000476988.1:n.743-469G>A
|
|
|
ENST00000475477.5:c.*82-469G>A
|
ENSP00000476854.1:n.*82-469G>A
|
|
|
NM_000778.3:c.1223-259G>A
|
NP_000769.2:n.1223-259G>A
|
|
|
XM_005270539.1:c.929-259G>A
|
XP_005270596.1:n.929-259G>A
|
|
|
XM_011540826.1:c.1241-259G>A
|
XP_011539128.1:n.1241-259G>A
|
|
|
XM_011540827.1:c.947-259G>A
|
XP_011539129.1:n.947-259G>A
|
|
|
XM_011540828.1:c.929-259G>A
|
XP_011539130.1:n.929-259G>A
|
|
|
XR_246241.1:n.1127-259G>A
|
|
|
|
XR_246242.1:n.1111-259G>A
|
|
|
|
NM_001319155.1:c.1127-259G>A
|
NP_001306084.1:n.1127-259G>A
|
|
|
NM_001363587.1:c.929-259G>A
|
NP_001350516.1:n.929-259G>A
|
|
|
NR_134988.1:n.928-259G>A
|
|
|
|
NR_134989.1:n.1119-259G>A
|
|
|
|
NR_134990.1:n.1178-469G>A
|
|
|
|
NR_134991.1:n.1100-259G>A
|
|
|
|
NR_134992.1:n.794-469G>A
|
|
|
|
NR_134993.1:n.928-469G>A
|
|
|
|
NR_134994.1:n.1135-259G>A
|
|
|
|
XM_017000465.1:c.911-259G>A
|
XP_016855954.1:n.911-259G>A
|
|
|
XR_001737005.1:n.1266-469G>A
|
|
|
|
NM_000778.4:c.1223-259G>A
MANE Select
|
NP_000769.2:n.1223-259G>A
|
|
|
NM_001319155.2:c.1127-259G>A
|
NP_001306084.1:n.1127-259G>A
|
|
|
NM_001363587.2:c.929-259G>A
|
NP_001350516.1:n.929-259G>A
|
|
|
NR_134988.2:n.920-259G>A
|
|
|
|
NR_134989.2:n.1111-259G>A
|
|
|
|
NR_134990.2:n.1170-469G>A
|
|
|
|
NR_134991.2:n.1092-259G>A
|
|
|
|
NR_134992.2:n.786-469G>A
|
|
|
|
NR_134993.2:n.920-469G>A
|
|
|
|
NR_134994.2:n.1127-259G>A
|
|
|
