ENST00000595866.2:c.138+2588C>T
|
ENSP00000469553.2:n.138+2588C>T
|
|
ENST00000698367.1:n.85+2588C>T
|
|
|
ENST00000698368.1:c.114+2775C>T
|
ENSP00000513686.1:n.114+2775C>T
|
|
ENST00000311069.6:c.24G>A
MANE Select
|
ENSP00000310585.4:p.Thr8=
|
|
ENST00000311069.5:c.24G>A
|
ENSP00000310585.4:p.Thr8=
|
|
ENST00000595866.1:c.136+2588C>T
|
|
|
ENST00000598664.5:c.51+2588C>T
|
ENSP00000472796.1:n.51+2588C>T
|
|
ENST00000599243.5:c.*183+1385C>T
|
ENSP00000470078.1:n.*183+1385C>T
|
|
NM_174895.2:c.24G>A
|
NP_777555.1:p.Thr8=
|
|
XM_006722639.2:c.-60-604G>A
|
XP_006722702.1:n.-60-604G>A
|
|
XM_011527676.1:c.24G>A
|
XP_011525978.1:p.Thr8=
|
|
XM_006722639.3:c.-60-604G>A
|
XP_006722702.1:n.-60-604G>A
|
|
XM_017026249.2:c.187G>A
|
XP_016881738.1:p.Gly63Arg
|
|
XM_017026250.2:c.187G>A
|
XP_016881739.1:p.Gly63Arg
|
|
XM_017026251.2:c.24G>A
|
XP_016881740.1:p.Thr8=
|
|
XM_017026252.2:c.-60-604G>A
|
XP_016881741.1:n.-60-604G>A
|
|
XM_024451346.1:c.187G>A
|
XP_024307114.1:p.Gly63Arg
|
|
NM_174895.3:c.24G>A
MANE Select
|
NP_777555.1:p.Thr8=
|
|