ENST00000311737.12:c.454+116A>G
(PRSS1)
MANE Select
|
ENSP00000308720.7:n.454+116A>G
|
|
ENST00000311737.11:c.454+116A>G
(PRSS1)
|
ENSP00000308720.7:n.454+116A>G
|
|
ENST00000463701.1:n.918+116A>G
(PRSS1)
|
|
|
ENST00000486171.5:c.496+116A>G
(PRSS1)
|
ENSP00000417854.1:n.496+116A>G
|
|
ENST00000492062.1:c.304+116A>G
(PRSS1)
|
ENSP00000419912.1:n.304+116A>G
|
|
ENST00000610416.2:c.370+30957A>G
(TRBC1)
|
ENSP00000482915.1:n.370+30957A>G
|
|
ENST00000612126.4:c.454+116A>G
(PRSS1)
|
ENSP00000479959.1:n.454+116A>G
|
|
ENST00000619214.4:c.424+116A>G
(PRSS1)
|
ENSP00000481361.1:n.424+116A>G
|
|
ENST00000633114.1:c.321+249A>G
(PRSS2)
|
ENSP00000487822.1:n.321+249A>G
|
|
ENST00000634019.1:c.82+3352A>G
(PRSS2)
|
ENSP00000488594.1:n.82+3352A>G
|
|
NM_002769.4:c.454+116A>G
(PRSS1)
|
NP_002760.1:n.454+116A>G
|
|
XM_011516411.1:c.1129+116A>G
(PRSS1)
|
XP_011514713.1:n.1129+116A>G
|
|
NM_002769.5:c.454+116A>G
(PRSS1)
MANE Select
|
NP_002760.1:n.454+116A>G
|
|
NR_172947.1:n.396+116A>G
(PRSS1)
|
|
|
NR_172948.1:n.393+116A>G
(PRSS1)
|
|
|
NR_172949.1:n.393+116A>G
(PRSS1)
|
|
|
NR_172950.1:n.307+116A>G
(PRSS1)
|
|
|
NR_172951.1:n.241+116A>G
(PRSS1)
|
|
|