ENST00000287936.9:c.1722+67T>C
MANE Select
|
ENSP00000287936.4:n.1722+67T>C
|
|
ENST00000679456.1:n.2559+67T>C
|
|
|
ENST00000680160.1:c.1722+67T>C
|
ENSP00000505315.1:n.1722+67T>C
|
|
ENST00000680940.1:c.1722+67T>C
|
ENSP00000505561.1:n.1722+67T>C
|
|
ENST00000681271.1:c.1722+67T>C
|
ENSP00000505805.1:n.1722+67T>C
|
|
ENST00000681410.1:c.1722+67T>C
|
ENSP00000506232.1:n.1722+67T>C
|
|
ENST00000681567.1:c.*2271+67T>C
|
ENSP00000506708.1:n.*2271+67T>C
|
|
ENST00000287936.8:c.1722+67T>C
|
ENSP00000287936.4:n.1722+67T>C
|
|
ENST00000343975.9:c.1564-84T>C
|
ENSP00000340816.5:n.1564-84T>C
|
|
ENST00000508070.1:n.102T>C
|
|
|
ENST00000511206.5:c.1722+67T>C
|
ENSP00000426745.1:n.1722+67T>C
|
|
NM_000859.2:c.1722+67T>C
|
NP_000850.1:n.1722+67T>C
|
|
NM_001130996.1:c.1564-84T>C
|
NP_001124468.1:n.1564-84T>C
|
|
XM_011543357.1:c.1782+67T>C
|
XP_011541659.1:n.1782+67T>C
|
|
XM_011543358.1:c.1722+67T>C
|
XP_011541660.1:n.1722+67T>C
|
|
XM_011543359.1:c.1624-84T>C
|
XP_011541661.1:n.1624-84T>C
|
|
NM_001364187.1:c.1722+67T>C
|
NP_001351116.1:n.1722+67T>C
|
|
NM_000859.3:c.1722+67T>C
MANE Select
|
NP_000850.1:n.1722+67T>C
|
|
NM_001130996.2:c.1564-84T>C
|
NP_001124468.1:n.1564-84T>C
|
|