ENST00000485511.6:c.523-7C>T
(PPP2R5D)
MANE Select
|
ENSP00000417963.1:n.523-7C>T
|
|
ENST00000676174.1:n.182-7C>T
(PPP2R5D)
|
|
|
ENST00000230402.10:c.*204-7C>T
(PPP2R5D)
|
ENSP00000230402.6:n.*204-7C>T
|
|
ENST00000394110.7:c.427-7C>T
(PPP2R5D)
|
ENSP00000377669.3:n.427-7C>T
|
|
ENST00000461010.5:c.205-7C>T
(PPP2R5D)
|
ENSP00000420674.1:n.205-7C>T
|
|
ENST00000467447.1:n.100-7C>T
(PPP2R5D)
|
|
|
ENST00000470467.5:c.281-7C>T
(PPP2R5D)
|
|
|
ENST00000472118.5:c.499-7C>T
(PPP2R5D)
|
ENSP00000420550.1:n.499-7C>T
|
|
ENST00000485511.5:c.523-7C>T
(PPP2R5D)
|
ENSP00000417963.1:n.523-7C>T
|
|
NM_001270476.1:c.70-7C>T
(PPP2R5D)
|
NP_001257405.1:n.70-7C>T
|
|
NM_006245.3:c.523-7C>T
(PPP2R5D)
|
NP_006236.1:n.523-7C>T
|
|
NM_180976.2:c.427-7C>T
(PPP2R5D)
|
NP_851307.1:n.427-7C>T
|
|
NM_180977.2:c.205-7C>T
(PPP2R5D)
|
NP_851308.1:n.205-7C>T
|
|
XM_005249123.1:c.367+5737G>A
(MEA1)
|
XP_005249180.1:n.367+5737G>A
|
|
XM_017010868.1:c.367+5737G>A
(MEA1)
|
XP_016866357.1:n.367+5737G>A
|
|
NM_006245.4:c.523-7C>T
(PPP2R5D)
MANE Select
|
NP_006236.1:n.523-7C>T
|
|
NM_001270476.2:c.70-7C>T
(PPP2R5D)
|
NP_001257405.1:n.70-7C>T
|
|
NM_180976.3:c.427-7C>T
(PPP2R5D)
|
NP_851307.1:n.427-7C>T
|
|
NM_180977.3:c.205-7C>T
(PPP2R5D)
|
NP_851308.1:n.205-7C>T
|
|