ENST00000449291.7:c.1554+32C>G
MANE Select
|
ENSP00000401508.2:n.1554+32C>G
|
|
ENST00000340490.7:c.1586C>G
|
ENSP00000341136.3:p.Pro529Arg
|
|
ENST00000426292.7:c.1515+32C>G
|
ENSP00000390949.3:n.1515+32C>G
|
|
ENST00000435154.7:c.*210C>G
|
ENSP00000405670.3:n.*210C>G
|
|
ENST00000449291.6:c.1554+32C>G
|
ENSP00000401508.2:n.1554+32C>G
|
|
ENST00000460623.5:c.525C>G
|
|
|
ENST00000464332.5:n.1098+32C>G
|
|
|
ENST00000498076.5:n.333+32C>G
|
|
|
ENST00000529179.1:n.338+32C>G
|
|
|
NM_001286829.1:c.1515+32C>G
|
NP_001273758.1:n.1515+32C>G
|
|
NM_145201.5:c.1554+32C>G
|
NP_660202.3:n.1554+32C>G
|
|
XM_011517377.1:c.1292-54C>G
|
XP_011515679.1:n.1292-54C>G
|
|
NM_001363145.1:c.1473+32C>G
|
NP_001350074.1:n.1473+32C>G
|
|
NM_001363146.1:c.870+32C>G
|
NP_001350075.1:n.870+32C>G
|
|
XM_017013975.2:c.1805C>G
|
XP_016869464.1:p.Pro602Arg
|
|
XM_017013976.2:c.1773+32C>G
|
XP_016869465.1:n.1773+32C>G
|
|
XM_017013977.2:c.1505C>G
|
XP_016869466.1:p.Pro502Arg
|
|
XM_017013978.2:c.1511-54C>G
|
XP_016869467.1:n.1511-54C>G
|
|
XM_017013979.2:c.902C>G
|
XP_016869468.1:p.Pro301Arg
|
|
XM_024447332.1:c.929-54C>G
|
XP_024303100.1:n.929-54C>G
|
|
XM_024447333.1:c.821C>G
|
XP_024303101.1:p.Pro274Arg
|
|
NM_145201.6:c.1554+32C>G
MANE Select
|
NP_660202.3:n.1554+32C>G
|
|
NM_001286829.2:c.1515+32C>G
|
NP_001273758.1:n.1515+32C>G
|
|