ENST00000449291.7:c.1447-21T>C
MANE Select
|
ENSP00000401508.2:n.1447-21T>C
|
|
ENST00000340490.7:c.1447-21T>C
|
ENSP00000341136.3:n.1447-21T>C
|
|
ENST00000426292.7:c.1408-21T>C
|
ENSP00000390949.3:n.1408-21T>C
|
|
ENST00000435154.7:c.*50T>C
|
ENSP00000405670.3:n.*50T>C
|
|
ENST00000449291.6:c.1447-21T>C
|
ENSP00000401508.2:n.1447-21T>C
|
|
ENST00000460623.5:c.386-21T>C
|
|
|
ENST00000464332.5:n.991-21T>C
|
|
|
ENST00000498076.5:n.226-21T>C
|
|
|
ENST00000529179.1:n.210T>C
|
|
|
NM_001286829.1:c.1408-21T>C
|
NP_001273758.1:n.1408-21T>C
|
|
NM_145201.5:c.1447-21T>C
|
NP_660202.3:n.1447-21T>C
|
|
XM_011517377.1:c.1292-214T>C
|
XP_011515679.1:n.1292-214T>C
|
|
NM_001363145.1:c.1366-21T>C
|
NP_001350074.1:n.1366-21T>C
|
|
NM_001363146.1:c.763-21T>C
|
NP_001350075.1:n.763-21T>C
|
|
XM_017013975.2:c.1666-21T>C
|
XP_016869464.1:n.1666-21T>C
|
|
XM_017013976.2:c.1666-21T>C
|
XP_016869465.1:n.1666-21T>C
|
|
XM_017013977.2:c.1366-21T>C
|
XP_016869466.1:n.1366-21T>C
|
|
XM_017013978.2:c.1511-214T>C
|
XP_016869467.1:n.1511-214T>C
|
|
XM_017013979.2:c.763-21T>C
|
XP_016869468.1:n.763-21T>C
|
|
XM_024447332.1:c.929-214T>C
|
XP_024303100.1:n.929-214T>C
|
|
XM_024447333.1:c.682-21T>C
|
XP_024303101.1:n.682-21T>C
|
|
NM_145201.6:c.1447-21T>C
MANE Select
|
NP_660202.3:n.1447-21T>C
|
|
NM_001286829.2:c.1408-21T>C
|
NP_001273758.1:n.1408-21T>C
|
|