ENST00000427262.6:c.1487+113T>C
|
ENSP00000405052.1:n.1487+113T>C
|
|
ENST00000642232.1:c.1667+113T>C
|
ENSP00000494064.1:n.1667+113T>C
|
|
ENST00000643230.2:c.1667+113T>C
MANE Select
|
ENSP00000496491.1:n.1667+113T>C
|
|
ENST00000643441.1:n.1652+113T>C
|
|
|
ENST00000307792.7:c.1667+113T>C
|
ENSP00000303212.3:n.1667+113T>C
|
|
ENST00000427262.5:c.1487+113T>C
|
ENSP00000405052.1:n.1487+113T>C
|
|
NM_001178129.1:c.1487+113T>C
|
NP_001171600.1:n.1487+113T>C
|
|
NM_012431.2:c.1667+113T>C
|
NP_036563.1:n.1667+113T>C
|
|
XM_011516715.1:c.1667+113T>C
|
XP_011515017.1:n.1667+113T>C
|
|
NM_012431.3:c.1667+113T>C
MANE Select
|
NP_036563.1:n.1667+113T>C
|
|
NM_001178129.2:c.1487+113T>C
|
NP_001171600.1:n.1487+113T>C
|
|