ENST00000531380.2:c.1476C>T
(FZD4)
MANE Select
|
ENSP00000434034.1:p.Gly492=
|
|
ENST00000528769.5:n.337G>A
(PRSS23)
|
|
|
ENST00000531380.1:c.1476C>T
(FZD4)
|
ENSP00000434034.1:p.Gly492=
|
|
ENST00000531521.1:n.451G>A
(PRSS23)
|
|
|
ENST00000532234.5:c.*273G>A
(PRSS23)
|
ENSP00000436676.1:n.*273G>A
|
|
ENST00000533902.2:c.271G>A
(PRSS23)
|
ENSP00000437268.1:p.Ala91Thr
|
|
NM_012193.3:c.1476C>T
(FZD4)
|
NP_036325.2:p.Gly492=
|
|
NR_120591.1:n.945G>A
(PRSS23)
|
|
|
NR_120592.1:n.694G>A
(PRSS23)
|
|
|
NR_120591.2:n.643G>A
(PRSS23)
|
|
|
NR_120592.2:n.392G>A
(PRSS23)
|
|
|
NM_012193.4:c.1476C>T
(FZD4)
MANE Select
|
NP_036325.2:p.Gly492=
|
|
NR_120591.3:n.643G>A
(PRSS23)
|
|
|