|
NM_002769.5:c.342C>T
(PRSS1)
MANE Select
|
NP_002760.1:p.Ser114=
|
|
ENST00000311737.12:c.342C>T
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Ser114=
|
|
NM_002769.4:c.342C>T
(PRSS1)
|
NP_002760.1:p.Ser114=
|
|
NR_172947.1:n.284C>T
(PRSS1)
|
|
|
NR_172948.1:n.281C>T
(PRSS1)
|
|
|
NR_172949.1:n.281C>T
(PRSS1)
|
|
|
NR_172950.1:n.195C>T
(PRSS1)
|
|
|
NR_172951.1:n.140-11C>T
(PRSS1)
|
|
|
ENST00000311737.11:c.342C>T
(PRSS1)
|
ENSP00000308720.7:p.Ser114=
|
|
ENST00000463701.1:n.806C>T
(PRSS1)
|
|
|
ENST00000485223.1:n.1340C>T
(PRSS1)
|
|
|
ENST00000486171.5:c.384C>T
(PRSS1)
|
ENSP00000417854.1:p.Ser128=
|
|
ENST00000492062.1:c.192C>T
(PRSS1)
|
ENSP00000419912.1:p.Ser64=
|
|
ENST00000610416.2:c.370+30729C>T
(TRBC1)
|
ENSP00000482915.1:n.370+30729C>T
|
|
ENST00000612126.4:c.342C>T
(PRSS1)
|
ENSP00000479959.1:p.Ser114=
|
|
ENST00000619214.4:c.312C>T
(PRSS1)
|
ENSP00000481361.1:p.Ser104=
|
|
ENST00000633114.1:c.321+21C>T
(PRSS2)
|
ENSP00000487822.1:n.321+21C>T
|
|
ENST00000634019.1:c.82+3124C>T
(PRSS2)
|
ENSP00000488594.1:n.82+3124C>T
|
|
XM_011516411.1:c.1017C>T
(PRSS1)
|
XP_011514713.1:p.Ser339=
|
