ENST00000695651.1:n.1118G>C
|
|
|
ENST00000695652.1:c.2647G>C
|
ENSP00000512083.1:p.Gly883Arg
|
|
ENST00000695653.1:c.679G>C
|
ENSP00000512084.1:p.Gly227Arg
|
|
ENST00000695654.1:c.1894G>C
|
ENSP00000512085.1:p.Gly632Arg
|
|
ENST00000695655.1:c.1711G>C
|
ENSP00000512086.1:n.1711G>C
|
|
ENST00000695692.1:n.2134G>C
|
|
|
ENST00000245907.11:c.2770G>C
MANE Select
|
ENSP00000245907.4:p.Gly924Arg
|
|
ENST00000245907.10:c.2770G>C
|
ENSP00000245907.4:p.Gly924Arg
|
|
ENST00000594005.1:n.346G>C
|
|
|
NM_000064.3:c.2770G>C
|
NP_000055.2:p.Gly924Arg
|
|
NM_000064.4:c.2770G>C
MANE Select
|
NP_000055.2:p.Gly924Arg
|
|