ENST00000371270.6:c.1150-1651T>C
MANE Select
|
ENSP00000360317.3:n.1150-1651T>C
|
|
ENST00000371270.5:c.1150-1651T>C
|
ENSP00000360317.3:n.1150-1651T>C
|
|
ENST00000479946.2:n.1492+233T>C
|
|
|
ENST00000490994.6:c.*936-1651T>C
|
ENSP00000433314.1:n.*936-1651T>C
|
|
ENST00000525991.5:c.*725-1651T>C
|
ENSP00000433842.1:n.*725-1651T>C
|
|
ENST00000526814.5:n.1405-1651T>C
|
|
|
ENST00000527420.5:c.*6+233T>C
|
ENSP00000433191.1:n.*6+233T>C
|
|
ENST00000527953.5:n.1443+233T>C
|
|
|
ENST00000533320.5:n.1384-1651T>C
|
|
|
ENST00000535898.5:c.844-1651T>C
|
ENSP00000445062.1:n.844-1651T>C
|
|
ENST00000539050.5:c.940-1651T>C
|
ENSP00000442343.2:n.940-1651T>C
|
|
ENST00000623108.3:c.940-1651T>C
|
ENSP00000485110.1:n.940-1651T>C
|
|
NM_000770.3:c.1150-1651T>C
MANE Select
|
NP_000761.3:n.1150-1651T>C
|
|
NM_001198853.1:c.940-1651T>C
|
NP_001185782.1:n.940-1651T>C
|
|
NM_001198854.1:c.844-1651T>C
|
NP_001185783.1:n.844-1651T>C
|
|
NM_001198855.1:c.940-1651T>C
|
NP_001185784.1:n.940-1651T>C
|
|
XR_945610.1:n.1284+233T>C
|
|
|