ENST00000305264.8:c.970C>A
MANE Select
|
ENSP00000302967.3:p.Pro324Thr
|
|
ENST00000305264.7:c.970C>A
|
ENSP00000302967.3:p.Pro324Thr
|
|
ENST00000459727.5:n.233+172C>A
|
|
|
ENST00000467533.5:n.599+172C>A
|
|
|
ENST00000469207.5:n.49C>A
|
|
|
ENST00000469550.6:n.1043C>A
|
|
|
ENST00000486618.1:n.464C>A
|
|
|
ENST00000491581.5:n.184C>A
|
|
|
ENST00000492407.1:n.767+172C>A
|
|
|
NM_003883.3:c.970C>A
|
NP_003874.2:p.Pro324Thr
|
|
XM_011537697.1:c.409C>A
|
XP_011535999.1:p.Pro137Thr
|
|
XR_944336.1:n.1055C>A
|
|
|
NM_001355039.1:c.970C>A
|
NP_001341968.1:p.Pro324Thr
|
|
NM_001355040.1:c.511C>A
|
NP_001341969.1:p.Pro171Thr
|
|
NM_001355041.1:c.409C>A
|
NP_001341970.1:p.Pro137Thr
|
|
NR_149164.1:n.1036C>A
|
|
|
NR_149165.1:n.918C>A
|
|
|
NR_149166.1:n.843+172C>A
|
|
|
NR_149167.1:n.1011+172C>A
|
|
|
NR_149168.1:n.1061C>A
|
|
|
NR_149169.1:n.1061C>A
|
|
|
NM_003883.4:c.970C>A
MANE Select
|
NP_003874.2:p.Pro324Thr
|
|
NM_001355039.2:c.970C>A
|
NP_001341968.1:p.Pro324Thr
|
|
NR_149167.2:n.1004+172C>A
|
|
|
NM_001355040.2:c.511C>A
|
NP_001341969.1:p.Pro171Thr
|
|
NM_001355041.2:c.409C>A
|
NP_001341970.1:p.Pro137Thr
|
|
NR_149164.2:n.1029C>A
|
|
|
NR_149165.2:n.911C>A
|
|
|
NR_149166.2:n.836+172C>A
|
|
|
NR_149168.2:n.1054C>A
|
|
|
NR_149169.2:n.1054C>A
|
|
|