ENST00000280097.5:c.191-12656G>T
MANE Select
|
ENSP00000280097.3:n.191-12656G>T
|
|
ENST00000280097.4:c.191-12656G>T
|
ENSP00000280097.3:n.191-12656G>T
|
|
ENST00000410115.5:c.191-12656G>T
|
ENSP00000386940.1:n.191-12656G>T
|
|
ENST00000467390.5:n.203-12656G>T
|
|
|
ENST00000475675.5:c.*456-3554G>T
|
ENSP00000419415.1:n.*456-3554G>T
|
|
ENST00000480534.1:n.169-303G>T
|
|
|
ENST00000485653.1:n.123-12656G>T
|
|
|
NM_006895.2:c.191-12656G>T
|
NP_008826.1:n.191-12656G>T
|
|
XM_011511063.1:c.89-12656G>T
|
XP_011509365.1:n.89-12656G>T
|
|
XM_011511064.1:c.-188-12656G>T
|
XP_011509366.1:n.-188-12656G>T
|
|
XM_011511064.2:c.-188-12656G>T
|
XP_011509366.1:n.-188-12656G>T
|
|
XM_017003948.1:c.89-12656G>T
|
XP_016859437.1:n.89-12656G>T
|
|
XM_017003949.2:c.191-12656G>T
|
XP_016859438.1:n.191-12656G>T
|
|
XR_001739719.1:n.1040-7583C>A
|
|
|
XR_002959286.1:n.578-12656G>T
|
|
|
NM_006895.3:c.191-12656G>T
MANE Select
|
NP_008826.1:n.191-12656G>T
|
|