ENST00000647358.2:c.1284+182C>T
MANE Select
|
ENSP00000494162.1:n.1284+182C>T
|
|
ENST00000270279.7:c.1284+182C>T
|
ENSP00000270279.3:n.1284+182C>T
|
|
ENST00000341505.4:c.1146+182C>T
|
ENSP00000340250.4:n.1146+182C>T
|
|
NM_001130852.1:c.1146+182C>T
|
NP_001124324.1:n.1146+182C>T
|
|
NM_012116.3:c.1284+182C>T
|
NP_036248.3:n.1284+182C>T
|
|
XM_005258696.2:c.1284+182C>T
|
XP_005258753.1:n.1284+182C>T
|
|
XM_011526688.1:c.1284+182C>T
|
XP_011524990.1:n.1284+182C>T
|
|
XM_011526689.1:c.1146+182C>T
|
XP_011524991.1:n.1146+182C>T
|
|
XR_935783.1:n.1231+182C>T
|
|
|
NM_012116.4:c.1284+182C>T
MANE Select
|
NP_036248.3:n.1284+182C>T
|
|
XM_005258696.3:c.1284+182C>T
|
XP_005258753.1:n.1284+182C>T
|
|
XM_011526688.2:c.1284+182C>T
|
XP_011524990.1:n.1284+182C>T
|
|
XM_011526689.2:c.1146+182C>T
|
XP_011524991.1:n.1146+182C>T
|
|
XR_935783.2:n.1236+182C>T
|
|
|