ENST00000502274.2:c.2752G>T
|
|
|
ENST00000515425.6:c.2856G>T
MANE Select
|
ENSP00000423660.1:p.Arg952Ser
|
|
ENST00000675793.1:c.*2140G>T
|
ENSP00000502039.1:n.*2140G>T
|
|
ENST00000676056.1:c.*2366G>T
|
ENSP00000501827.1:n.*2366G>T
|
|
ENST00000323829.9:c.*2244G>T
|
ENSP00000313025.5:n.*2244G>T
|
|
ENST00000504517.5:c.2386G>T
|
ENSP00000421779.1:n.2386G>T
|
|
ENST00000504690.5:c.2856G>T
|
ENSP00000425627.1:p.Arg952Ser
|
|
ENST00000510779.1:c.1906G>T
|
|
|
ENST00000511307.5:c.*2636G>T
|
ENSP00000421420.1:n.*2636G>T
|
|
ENST00000512049.5:c.2835G>T
|
ENSP00000421860.1:p.Arg945Ser
|
|
ENST00000513604.5:c.*2244G>T
|
ENSP00000423111.1:n.*2244G>T
|
|
ENST00000515425.5:c.2856G>T
|
ENSP00000423660.1:p.Arg952Ser
|
|
NM_024577.3:c.2856G>T , LRG_269t1:c.2856G>T
|
NP_078853.2:p.Arg952Ser
|
|
NM_024577.4:c.2856G>T
MANE Select
|
NP_078853.2:p.Arg952Ser
|
|