ENST00000297784.10:c.1695+78A>G
MANE Select
|
ENSP00000297784.6:n.1695+78A>G
|
|
ENST00000644967.1:c.1257+78A>G
|
ENSP00000496159.1:n.1257+78A>G
|
|
ENST00000645053.1:c.1257+78A>G
|
ENSP00000493838.1:n.1257+78A>G
|
|
ENST00000645208.2:c.1695+78A>G
|
ENSP00000494684.1:n.1695+78A>G
|
|
ENST00000645773.1:c.1569+78A>G
|
ENSP00000493698.1:n.1569+78A>G
|
|
ENST00000645787.1:n.1838+78A>G
|
|
|
ENST00000646619.1:c.1257+78A>G
|
ENSP00000493726.1:n.1257+78A>G
|
|
ENST00000651183.1:c.1257+78A>G
|
ENSP00000498723.1:n.1257+78A>G
|
|
ENST00000297784.9:c.1695+78A>G
|
ENSP00000297784.5:n.1695+78A>G
|
|
ENST00000340019.4:c.1695+78A>G
|
ENSP00000341433.3:n.1695+78A>G
|
|
ENST00000486417.5:n.319+78A>G
|
|
|
NM_138691.2:c.1695+78A>G
|
NP_619636.2:n.1695+78A>G
|
|
XM_011518213.1:c.2283+78A>G
|
XP_011516515.1:n.2283+78A>G
|
|
XM_017014256.1:c.1698+78A>G
|
XP_016869745.1:n.1698+78A>G
|
|
NM_138691.3:c.1695+78A>G
MANE Select
|
NP_619636.2:n.1695+78A>G
|
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