ENST00000649046.1:c.12295+201T>C
MANE Select
|
ENSP00000496870.1:n.12295+201T>C
|
|
ENST00000649153.1:c.3195+201T>C
|
|
|
ENST00000650252.1:c.1323+201T>C
|
ENSP00000496887.1:n.1323+201T>C
|
|
ENST00000263816.7:c.12295+201T>C
|
ENSP00000263816.3:n.12295+201T>C
|
|
NM_004525.2:c.12295+201T>C
|
NP_004516.2:n.12295+201T>C
|
|
XM_011511183.1:c.12166+201T>C
|
XP_011509485.1:n.12166+201T>C
|
|
XM_011511184.1:c.10006+201T>C
|
XP_011509486.1:n.10006+201T>C
|
|
NM_004525.3:c.12295+201T>C
MANE Select
|
NP_004516.2:n.12295+201T>C
|
|
XM_011511183.3:c.12166+201T>C
|
XP_011509485.1:n.12166+201T>C
|
|
XM_011511184.2:c.10006+201T>C
|
XP_011509486.1:n.10006+201T>C
|
|