ENST00000376810.6:c.*1268G>A
MANE Select
|
ENSP00000366006.5:n.*1268G>A
|
|
ENST00000376804.2:c.530-7474G>A
|
ENSP00000366000.1:n.530-7474G>A
|
|
ENST00000376810.5:c.*1268G>A
|
ENSP00000366006.5:n.*1268G>A
|
|
ENST00000483738.1:c.216+1667G>A
|
ENSP00000473453.1:n.216+1667G>A
|
|
ENST00000486588.6:c.261+1667G>A
|
ENSP00000473612.1:n.261+1667G>A
|
|
NM_013319.2:c.*1268G>A
|
NP_037451.1:n.*1268G>A
|
|
XM_006710590.2:c.618+1667G>A
|
XP_006710653.1:n.618+1667G>A
|
|
XM_011541304.1:c.530-7474G>A
|
XP_011539606.1:n.530-7474G>A
|
|
XR_946616.1:n.952+1667G>A
|
|
|
NM_001330349.1:c.618+1667G>A
|
NP_001317278.1:n.618+1667G>A
|
|
NM_001330350.1:c.530-7474G>A
|
NP_001317279.1:n.530-7474G>A
|
|
XR_946616.3:n.952+1667G>A
|
|
|
NM_001330349.2:c.618+1667G>A
|
NP_001317278.1:n.618+1667G>A
|
|
NM_001330350.2:c.530-7474G>A
|
NP_001317279.1:n.530-7474G>A
|
|
NM_013319.3:c.*1268G>A
MANE Select
|
NP_037451.1:n.*1268G>A
|
|