ENST00000332896.8:c.525C>A
MANE Select
|
ENSP00000327647.3:p.Ala175=
|
|
ENST00000332896.7:c.525C>A
|
ENSP00000327647.3:p.Ala175=
|
|
ENST00000542893.2:c.525C>A
|
ENSP00000439068.2:p.Ala175=
|
|
ENST00000548330.1:n.910C>A
|
|
|
ENST00000548483.5:c.299-43854C>A
|
ENSP00000448685.1:n.299-43854C>A
|
|
ENST00000550030.1:n.325C>A
|
|
|
ENST00000551065.5:c.299-9123C>A
|
ENSP00000448425.1:n.299-9123C>A
|
|
ENST00000609189.1:n.301C>A
|
|
|
NM_003805.3:c.525C>A
|
NP_003796.1:p.Ala175=
|
|
XM_005269211.3:c.299-43854C>A
|
XP_005269268.1:n.299-43854C>A
|
|
NM_001320099.1:c.525C>A
|
NP_001307028.1:p.Ala175=
|
|
NM_001320100.1:c.299-43854C>A
|
NP_001307029.1:n.299-43854C>A
|
|
NM_003805.4:c.525C>A
|
NP_003796.1:p.Ala175=
|
|
NR_135147.1:n.407-9123C>A
|
|
|
XM_017020144.1:c.299-9123C>A
|
XP_016875633.1:n.299-9123C>A
|
|
XR_001748910.1:n.430-9123C>A
|
|
|
NM_003805.5:c.525C>A
MANE Select
|
NP_003796.1:p.Ala175=
|
|
NM_001320099.2:c.525C>A
|
NP_001307028.1:p.Ala175=
|
|
NM_001320100.2:c.299-43854C>A
|
NP_001307029.1:n.299-43854C>A
|
|
NR_135147.2:n.403-9123C>A
|
|
|