ENST00000382329.2:c.-151G>T
|
ENSP00000371766.2:n.-151G>T
|
|
ENST00000682121.1:n.166-14834G>T
|
|
|
ENST00000684166.1:n.163G>T
|
|
|
ENST00000684384.1:n.163G>T
|
|
|
ENST00000432829.7:c.54G>T
MANE Select
|
ENSP00000394888.3:p.Arg18Ser
|
|
ENST00000432829.6:c.54G>T
|
ENSP00000394888.3:p.Arg18Ser
|
|
ENST00000454469.6:n.163G>T
|
|
|
ENST00000469197.5:c.54G>T
|
ENSP00000418587.1:p.Arg18Ser
|
|
ENST00000479404.5:c.-151G>T
|
ENSP00000417082.1:n.-151G>T
|
|
ENST00000524396.5:c.*17G>T
|
ENSP00000436628.1:n.*17G>T
|
|
NM_203447.3:c.54G>T , LRG_196t1:c.54G>T
|
NP_982272.2:p.Arg18Ser
|
|
XM_011518045.1:c.-151G>T
|
XP_011516347.1:n.-151G>T
|
|
XM_011518047.1:c.-151G>T
|
XP_011516349.1:n.-151G>T
|
|
XR_929404.1:n.88+1278C>A
|
|
|
XR_929406.1:n.1333+2657C>A
|
|
|
XM_011518045.3:c.-151G>T
|
XP_011516347.1:n.-151G>T
|
|
XM_011518047.3:c.-151G>T
|
XP_011516349.1:n.-151G>T
|
|
XM_017015173.1:c.-151G>T
|
XP_016870662.1:n.-151G>T
|
|
NM_203447.4:c.54G>T
MANE Select
|
NP_982272.2:p.Arg18Ser
|
|