ENST00000311737.12:c.440C>A
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Thr147Asn
|
|
ENST00000311737.11:c.440C>A
(PRSS1)
|
ENSP00000308720.7:p.Thr147Asn
|
|
ENST00000463701.1:n.904C>A
(PRSS1)
|
|
|
ENST00000486171.5:c.482C>A
(PRSS1)
|
ENSP00000417854.1:p.Thr161Asn
|
|
ENST00000492062.1:c.290C>A
(PRSS1)
|
ENSP00000419912.1:p.Thr97Asn
|
|
ENST00000610416.2:c.370+30827C>A
(TRBC1)
|
ENSP00000482915.1:n.370+30827C>A
|
|
ENST00000612126.4:c.440C>A
(PRSS1)
|
ENSP00000479959.1:p.Thr147Asn
|
|
ENST00000619214.4:c.410C>A
(PRSS1)
|
ENSP00000481361.1:p.Thr137Asn
|
|
ENST00000633114.1:c.321+119C>A
(PRSS2)
|
ENSP00000487822.1:n.321+119C>A
|
|
ENST00000634019.1:c.82+3222C>A
(PRSS2)
|
ENSP00000488594.1:n.82+3222C>A
|
|
NM_002769.4:c.440C>A
(PRSS1)
|
NP_002760.1:p.Thr147Asn
|
|
XM_011516411.1:c.1115C>A
(PRSS1)
|
XP_011514713.1:p.Thr372Asn
|
|
NM_002769.5:c.440C>A
(PRSS1)
MANE Select
|
NP_002760.1:p.Thr147Asn
|
|
NR_172947.1:n.382C>A
(PRSS1)
|
|
|
NR_172948.1:n.379C>A
(PRSS1)
|
|
|
NR_172949.1:n.379C>A
(PRSS1)
|
|
|
NR_172950.1:n.293C>A
(PRSS1)
|
|
|
NR_172951.1:n.227C>A
(PRSS1)
|
|
|