ENST00000310109.5:c.466+62G>T
MANE Select
|
ENSP00000309463.4:n.466+62G>T
|
|
ENST00000310109.4:c.466+62G>T
|
ENSP00000309463.4:n.466+62G>T
|
|
ENST00000527115.1:c.116+24G>T
|
|
|
ENST00000528085.1:c.181+291G>T
|
|
|
NM_001144869.1:c.466+62G>T
|
NP_001138341.1:n.466+62G>T
|
|
XM_011545021.1:c.504+24G>T
|
XP_011543323.1:n.504+24G>T
|
|
NM_001144869.2:c.466+62G>T
|
NP_001138341.1:n.466+62G>T
|
|
NM_001329941.1:c.504+24G>T
|
NP_001316870.1:n.504+24G>T
|
|
NM_001329942.1:c.237+291G>T
|
NP_001316871.1:n.237+291G>T
|
|
NM_001144869.3:c.466+62G>T
MANE Select
|
NP_001138341.1:n.466+62G>T
|
|
NM_001329941.2:c.504+24G>T
|
NP_001316870.1:n.504+24G>T
|
|
NM_001329942.2:c.237+291G>T
|
NP_001316871.1:n.237+291G>T
|
|