ENST00000372563.2:c.1045-9C>T
MANE Select
|
ENSP00000361644.1:n.1045-9C>T
|
|
ENST00000327674.8:c.1045-9C>T
|
ENSP00000329374.4:n.1045-9C>T
|
|
ENST00000372563.1:c.1045-9C>T
|
ENSP00000361644.1:n.1045-9C>T
|
|
ENST00000487487.1:n.370C>T
|
|
|
NM_000354.5:c.1045-9C>T
|
NP_000345.2:n.1045-9C>T
|
|
XM_005262180.3:c.1097C>T
|
XP_005262237.1:p.Pro366Leu
|
|
XM_006724683.1:c.1066C>T
|
XP_006724746.1:p.Pro356Ser
|
|
XM_005262180.4:c.1097C>T
|
XP_005262237.1:p.Pro366Leu
|
|
XM_006724683.2:c.1066C>T
|
XP_006724746.1:p.Pro356Ser
|
|
NM_000354.6:c.1045-9C>T
MANE Select
|
NP_000345.2:n.1045-9C>T
|
|