ENST00000288710.7:c.2063+152A>G
MANE Select
|
ENSP00000288710.2:n.2063+152A>G
|
|
ENST00000649059.1:c.1909+152A>G
|
|
|
ENST00000288710.6:c.2063+152A>G
|
ENSP00000288710.2:n.2063+152A>G
|
|
NM_145038.3:c.2063+152A>G
|
NP_659475.2:n.2063+152A>G
|
|
NM_145038.4:c.2063+152A>G
|
NP_659475.2:n.2063+152A>G
|
|
XM_005264637.3:c.1445+152A>G
|
XP_005264694.1:n.1445+152A>G
|
|
XM_005264638.3:c.1043+152A>G
|
XP_005264695.1:n.1043+152A>G
|
|
XM_017005271.1:c.1043+152A>G
|
XP_016860760.1:n.1043+152A>G
|
|
XM_024453218.1:c.1043+152A>G
|
XP_024308986.1:n.1043+152A>G
|
|
NM_145038.5:c.2063+152A>G
MANE Select
|
NP_659475.2:n.2063+152A>G
|
|