ENST00000311737.12:c.442G>T
(PRSS1)
MANE Select
|
ENSP00000308720.7:p.Ala148Ser
|
|
ENST00000311737.11:c.442G>T
(PRSS1)
|
ENSP00000308720.7:p.Ala148Ser
|
|
ENST00000463701.1:n.906G>T
(PRSS1)
|
|
|
ENST00000486171.5:c.484G>T
(PRSS1)
|
ENSP00000417854.1:p.Ala162Ser
|
|
ENST00000492062.1:c.292G>T
(PRSS1)
|
ENSP00000419912.1:p.Ala98Ser
|
|
ENST00000610416.2:c.370+30829G>T
(TRBC1)
|
ENSP00000482915.1:n.370+30829G>T
|
|
ENST00000612126.4:c.442G>T
(PRSS1)
|
ENSP00000479959.1:p.Ala148Ser
|
|
ENST00000619214.4:c.412G>T
(PRSS1)
|
ENSP00000481361.1:p.Ala138Ser
|
|
ENST00000633114.1:c.321+121G>T
(PRSS2)
|
ENSP00000487822.1:n.321+121G>T
|
|
ENST00000634019.1:c.82+3224G>T
(PRSS2)
|
ENSP00000488594.1:n.82+3224G>T
|
|
NM_002769.4:c.442G>T
(PRSS1)
|
NP_002760.1:p.Ala148Ser
|
|
XM_011516411.1:c.1117G>T
(PRSS1)
|
XP_011514713.1:p.Ala373Ser
|
|
NM_002769.5:c.442G>T
(PRSS1)
MANE Select
|
NP_002760.1:p.Ala148Ser
|
|
NR_172947.1:n.384G>T
(PRSS1)
|
|
|
NR_172948.1:n.381G>T
(PRSS1)
|
|
|
NR_172949.1:n.381G>T
(PRSS1)
|
|
|
NR_172950.1:n.295G>T
(PRSS1)
|
|
|
NR_172951.1:n.229G>T
(PRSS1)
|
|
|