ENST00000311737.12:c.215G>C
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Arg72Thr
|
|
ENST00000311737.11:c.215G>C
(PRSS1)
|
ENSP00000308720.7:p.Arg72Thr
|
|
ENST00000463701.1:n.679G>C
(PRSS1)
|
|
|
ENST00000485223.1:n.1213G>C
(PRSS1)
|
|
|
ENST00000486171.5:c.257G>C
(PRSS1)
|
ENSP00000417854.1:p.Arg86Thr
|
|
ENST00000492062.1:c.65G>C
(PRSS1)
|
ENSP00000419912.1:p.Arg22Thr
|
|
ENST00000610416.2:c.370+30602G>C
(TRBC1)
|
ENSP00000482915.1:n.370+30602G>C
|
|
ENST00000612126.4:c.215G>C
(PRSS1)
|
ENSP00000479959.1:p.Arg72Thr
|
|
ENST00000619214.4:c.215G>C
(PRSS1)
|
ENSP00000481361.1:p.Arg72Thr
|
|
ENST00000633114.1:c.215G>C
(PRSS2)
|
ENSP00000487822.1:p.Arg72Thr
|
|
ENST00000634019.1:c.82+2997G>C
(PRSS2)
|
ENSP00000488594.1:n.82+2997G>C
|
|
NM_002769.4:c.215G>C
(PRSS1)
|
NP_002760.1:p.Arg72Thr
|
|
XM_011516411.1:c.890G>C
(PRSS1)
|
XP_011514713.1:p.Arg297Thr
|
|
NM_002769.5:c.215G>C
(PRSS1)
MANE Select
|
NP_002760.1:p.Arg72Thr
|
|
NR_172947.1:n.198-41G>C
(PRSS1)
|
|
|
NR_172948.1:n.198-44G>C
(PRSS1)
|
|
|
NR_172949.1:n.154G>C
(PRSS1)
|
|
|
NR_172950.1:n.68G>C
(PRSS1)
|
|
|
NR_172951.1:n.140-138G>C
(PRSS1)
|
|
|