ENST00000261647.10:c.184+27G>T
MANE Select
|
ENSP00000261647.5:n.184+27G>T
|
|
ENST00000261647.9:c.184+27G>T
|
ENSP00000261647.5:n.184+27G>T
|
|
ENST00000466729.5:c.249+27G>T
|
|
|
ENST00000470399.1:c.199+27G>T
|
ENSP00000465082.1:n.199+27G>T
|
|
ENST00000475723.5:c.231+27G>T
|
|
|
ENST00000497842.6:n.236G>T
|
|
|
ENST00000583704.1:n.209+27G>T
|
|
|
NM_001271420.1:c.-275+27G>T
|
NP_001258349.1:n.-275+27G>T
|
|
NM_017775.3:c.184+27G>T
|
NP_060245.3:n.184+27G>T
|
|
XM_011523950.1:c.184+27G>T
|
XP_011522252.1:n.184+27G>T
|
|
XM_017024801.2:c.184+27G>T
|
XP_016880290.2:n.184+27G>T
|
|
XM_017024802.2:c.184+27G>T
|
XP_016880291.2:n.184+27G>T
|
|
XM_024450814.1:c.184+27G>T
|
XP_024306582.1:n.184+27G>T
|
|
NM_017775.4:c.184+27G>T
MANE Select
|
NP_060245.3:n.184+27G>T
|
|
NM_001271420.2:c.-275+27G>T
|
NP_001258349.1:n.-275+27G>T
|
|