ENST00000695652.1:c.880+226G>C
|
ENSP00000512083.1:n.880+226G>C
|
|
ENST00000695654.1:c.127+226G>C
|
ENSP00000512085.1:n.127+226G>C
|
|
ENST00000695692.1:n.327+226G>C
|
|
|
ENST00000245907.11:c.1003+226G>C
MANE Select
|
ENSP00000245907.4:n.1003+226G>C
|
|
ENST00000245907.10:c.1003+226G>C
|
ENSP00000245907.4:n.1003+226G>C
|
|
ENST00000594270.5:n.127+226G>C
|
|
|
ENST00000595577.1:n.507+226G>C
|
|
|
ENST00000597442.5:n.253+226G>C
|
|
|
NM_000064.3:c.1003+226G>C
|
NP_000055.2:n.1003+226G>C
|
|
NM_000064.4:c.1003+226G>C
MANE Select
|
NP_000055.2:n.1003+226G>C
|
|