ENST00000381340.8:c.3462+7957G>A
MANE Select
|
ENSP00000370744.3:n.3462+7957G>A
|
|
ENST00000381340.7:c.3462+7957G>A
|
ENSP00000370744.3:n.3462+7957G>A
|
|
NM_002223.2:c.3462+7957G>A
|
NP_002214.2:n.3462+7957G>A
|
|
NM_002223.3:c.3462+7957G>A
|
NP_002214.2:n.3462+7957G>A
|
|
XM_011520645.1:c.2910+7957G>A
|
XP_011518947.1:n.2910+7957G>A
|
|
XM_011520646.1:c.2529+7957G>A
|
XP_011518948.1:n.2529+7957G>A
|
|
XR_931288.1:n.3878+7957G>A
|
|
|
XM_017019266.1:c.3522+7957G>A
|
XP_016874755.1:n.3522+7957G>A
|
|
XM_017019267.1:c.3456+7957G>A
|
XP_016874756.1:n.3456+7957G>A
|
|
XM_017019269.2:c.3522+7957G>A
|
XP_016874758.1:n.3522+7957G>A
|
|
XR_001748686.2:n.3938+7957G>A
|
|
|
XR_001748687.1:n.3938+7957G>A
|
|
|
NM_002223.4:c.3462+7957G>A
MANE Select
|
NP_002214.2:n.3462+7957G>A
|
|