ENST00000316793.8:c.922+4527C>T
MANE Select

ENSP00000324270.2:p.=


ENST00000316793.7:c.922+4527C>T

ENSP00000324270.2:p.=


ENST00000472766.1:n.15614738G>A



NM_000916.3:c.922+4527C>T

NP_000907.2:p.=


XM_011533762.1:c.922+4527C>T

XP_011532064.1:p.=


XM_011533763.1:c.922+4527C>T

XP_011532065.1:p.=


NM_001354653.1:c.922+4527C>T

NP_001341582.1:p.=


NM_001354654.1:c.922+4527C>T

NP_001341583.1:p.=


NM_001354655.1:c.922+4527C>T

NP_001341584.1:p.=


NM_001354656.1:c.922+4527C>T

NP_001341585.1:p.=


NM_001354656.2:c.922+4527C>T

NP_001341585.1:p.=


NM_000916.4:c.922+4527C>T
MANE Select

NP_000907.2:p.=


NM_001354653.2:c.922+4527C>T

NP_001341582.1:p.=


NM_001354654.2:c.922+4527C>T

NP_001341583.1:p.=


NM_001354655.2:c.922+4527C>T

NP_001341584.1:p.=


NM_001354656.3:c.922+4527C>T

NP_001341585.1:p.=

