ENST00000311737.12:c.420C>G
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Leu140=
|
|
ENST00000311737.11:c.420C>G
(PRSS1)
|
ENSP00000308720.7:p.Leu140=
|
|
ENST00000463701.1:n.884C>G
(PRSS1)
|
|
|
ENST00000485223.1:n.1418C>G
(PRSS1)
|
|
|
ENST00000486171.5:c.462C>G
(PRSS1)
|
ENSP00000417854.1:p.Leu154=
|
|
ENST00000492062.1:c.270C>G
(PRSS1)
|
ENSP00000419912.1:p.Leu90=
|
|
ENST00000610416.2:c.370+30807C>G
(TRBC1)
|
ENSP00000482915.1:n.370+30807C>G
|
|
ENST00000612126.4:c.420C>G
(PRSS1)
|
ENSP00000479959.1:p.Leu140=
|
|
ENST00000619214.4:c.390C>G
(PRSS1)
|
ENSP00000481361.1:p.Leu130=
|
|
ENST00000633114.1:c.321+99C>G
(PRSS2)
|
ENSP00000487822.1:n.321+99C>G
|
|
ENST00000634019.1:c.82+3202C>G
(PRSS2)
|
ENSP00000488594.1:n.82+3202C>G
|
|
NM_002769.4:c.420C>G
(PRSS1)
|
NP_002760.1:p.Leu140=
|
|
XM_011516411.1:c.1095C>G
(PRSS1)
|
XP_011514713.1:p.Leu365=
|
|
NM_002769.5:c.420C>G
(PRSS1)
MANE Select
|
NP_002760.1:p.Leu140=
|
|
NR_172947.1:n.362C>G
(PRSS1)
|
|
|
NR_172948.1:n.359C>G
(PRSS1)
|
|
|
NR_172949.1:n.359C>G
(PRSS1)
|
|
|
NR_172950.1:n.273C>G
(PRSS1)
|
|
|
NR_172951.1:n.207C>G
(PRSS1)
|
|
|