ENST00000247933.9:c.1727+38T>C
|
ENSP00000247933.4:n.1727+38T>C
|
|
ENST00000514224.2:c.1727+38T>C
MANE Select
|
ENSP00000425081.2:n.1727+38T>C
|
|
ENST00000652070.1:n.1783+38T>C
|
|
|
ENST00000247933.8:c.1727+38T>C
|
ENSP00000247933.4:n.1727+38T>C
|
|
ENST00000514224.1:c.1331+38T>C
|
ENSP00000425081.1:n.1331+38T>C
|
|
ENST00000514417.1:n.157T>C
|
|
|
ENST00000514698.5:n.1838+34T>C
|
|
|
NM_000203.4:c.1727+38T>C
|
NP_000194.2:n.1727+38T>C
|
|
NR_110313.1:n.1819+34T>C
|
|
|
XM_006713882.2:c.1331+38T>C
|
XP_006713945.1:n.1331+38T>C
|
|
XM_011513459.1:c.1793+38T>C
|
XP_011511761.1:n.1793+38T>C
|
|
XM_011513460.1:c.1586+38T>C
|
XP_011511762.1:n.1586+38T>C
|
|
XM_011513461.1:c.1520+38T>C
|
XP_011511763.1:n.1520+38T>C
|
|
XM_011513462.1:c.1439+38T>C
|
XP_011511764.1:n.1439+38T>C
|
|
XM_011513463.1:c.1439+38T>C
|
XP_011511765.1:n.1439+38T>C
|
|
XR_924947.1:n.1987+34T>C
|
|
|
NM_000203.5:c.1727+38T>C
MANE Select
|
NP_000194.2:n.1727+38T>C
|
|
NM_001363576.1:c.1331+38T>C
|
NP_001350505.1:n.1331+38T>C
|
|
XM_011513461.2:c.1520+38T>C
|
XP_011511763.1:n.1520+38T>C
|
|
XM_017008163.1:c.767+38T>C
|
XP_016863652.1:n.767+38T>C
|
|