ENST00000485511.6:c.524T>A
(PPP2R5D)
MANE Select
|
ENSP00000417963.1:p.Phe175Tyr
|
|
ENST00000676174.1:n.183T>A
(PPP2R5D)
|
|
|
ENST00000230402.10:c.*205T>A
(PPP2R5D)
|
ENSP00000230402.6:n.*205T>A
|
|
ENST00000394110.7:c.428T>A
(PPP2R5D)
|
ENSP00000377669.3:p.Phe143Tyr
|
|
ENST00000461010.5:c.206T>A
(PPP2R5D)
|
ENSP00000420674.1:p.Phe69Tyr
|
|
ENST00000467447.1:n.101T>A
(PPP2R5D)
|
|
|
ENST00000470467.5:c.282T>A
(PPP2R5D)
|
|
|
ENST00000472118.5:c.500T>A
(PPP2R5D)
|
ENSP00000420550.1:p.Phe167Tyr
|
|
ENST00000485511.5:c.524T>A
(PPP2R5D)
|
ENSP00000417963.1:p.Phe175Tyr
|
|
NM_001270476.1:c.71T>A
(PPP2R5D)
|
NP_001257405.1:p.Phe24Tyr
|
|
NM_006245.3:c.524T>A
(PPP2R5D)
|
NP_006236.1:p.Phe175Tyr
|
|
NM_180976.2:c.428T>A
(PPP2R5D)
|
NP_851307.1:p.Phe143Tyr
|
|
NM_180977.2:c.206T>A
(PPP2R5D)
|
NP_851308.1:p.Phe69Tyr
|
|
XM_005249123.1:c.367+5729A>T
(MEA1)
|
XP_005249180.1:n.367+5729A>T
|
|
XM_017010868.1:c.367+5729A>T
(MEA1)
|
XP_016866357.1:n.367+5729A>T
|
|
NM_006245.4:c.524T>A
(PPP2R5D)
MANE Select
|
NP_006236.1:p.Phe175Tyr
|
|
NM_001270476.2:c.71T>A
(PPP2R5D)
|
NP_001257405.1:p.Phe24Tyr
|
|
NM_180976.3:c.428T>A
(PPP2R5D)
|
NP_851307.1:p.Phe143Tyr
|
|
NM_180977.3:c.206T>A
(PPP2R5D)
|
NP_851308.1:p.Phe69Tyr
|
|