ENST00000311737.12:c.80G>T
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Gly27Val
|
|
ENST00000311737.11:c.80G>T
(PRSS1)
|
ENSP00000308720.7:p.Gly27Val
|
|
ENST00000485223.1:n.54-35G>T
(PRSS1)
|
|
|
ENST00000486171.5:c.80G>T
(PRSS1)
|
ENSP00000417854.1:p.Gly27Val
|
|
ENST00000497041.1:n.84G>T
(PRSS1)
|
|
|
ENST00000610416.2:c.370+29408G>T
(TRBC1)
|
ENSP00000482915.1:n.370+29408G>T
|
|
ENST00000612126.4:c.80G>T
(PRSS1)
|
ENSP00000479959.1:p.Gly27Val
|
|
ENST00000619214.4:c.80G>T
(PRSS1)
|
ENSP00000481361.1:p.Gly27Val
|
|
ENST00000633114.1:c.80G>T
(PRSS2)
|
ENSP00000487822.1:p.Gly27Val
|
|
ENST00000634019.1:c.82+1803G>T
(PRSS2)
|
ENSP00000488594.1:n.82+1803G>T
|
|
NM_002769.4:c.80G>T
(PRSS1)
|
NP_002760.1:p.Gly27Val
|
|
XM_011516411.1:c.755G>T
(PRSS1)
|
XP_011514713.1:p.Gly252Val
|
|
NM_002769.5:c.80G>T
(PRSS1)
MANE Select
|
NP_002760.1:p.Gly27Val
|
|
NR_172947.1:n.93G>T
(PRSS1)
|
|
|
NR_172948.1:n.93G>T
(PRSS1)
|
|
|
NR_172949.1:n.54-35G>T
(PRSS1)
|
|
|
NR_172950.1:n.53+1070G>T
(PRSS1)
|
|
|
NR_172951.1:n.54-35G>T
(PRSS1)
|
|
|