ENST00000695651.1:n.2698+1G>C
|
|
|
ENST00000695653.1:c.2259+1G>C
|
ENSP00000512084.1:n.2259+1G>C
|
|
ENST00000695654.1:c.3375+1G>C
|
ENSP00000512085.1:n.3375+1G>C
|
|
ENST00000695689.1:c.321+1G>C
|
ENSP00000512101.1:n.321+1G>C
|
|
ENST00000695690.1:n.542G>C
|
|
|
ENST00000695691.1:n.542G>C
|
|
|
ENST00000245907.11:c.4350+1G>C
MANE Select
|
ENSP00000245907.4:n.4350+1G>C
|
|
ENST00000245907.10:c.4350+1G>C
|
ENSP00000245907.4:n.4350+1G>C
|
|
ENST00000596548.1:c.471+1G>C
|
ENSP00000469744.1:n.471+1G>C
|
|
ENST00000599899.5:n.1309+1G>C
|
|
|
ENST00000601008.1:c.242-3982G>C
|
ENSP00000471384.1:n.242-3982G>C
|
|
NM_000064.3:c.4350+1G>C
|
NP_000055.2:n.4350+1G>C
|
|
NM_000064.4:c.4350+1G>C
MANE Select
|
NP_000055.2:n.4350+1G>C
|
|