ENST00000695651.1:n.2141G>C
|
|
|
ENST00000695652.1:c.3670G>C
|
ENSP00000512083.1:p.Gly1224Arg
|
|
ENST00000695653.1:c.1702G>C
|
ENSP00000512084.1:p.Gly568Arg
|
|
ENST00000695654.1:c.2818G>C
|
ENSP00000512085.1:p.Gly940Arg
|
|
ENST00000695655.1:c.2734G>C
|
ENSP00000512086.1:n.2734G>C
|
|
ENST00000695692.1:n.3157G>C
|
|
|
ENST00000245907.11:c.3793G>C
MANE Select
|
ENSP00000245907.4:p.Gly1265Arg
|
|
ENST00000245907.10:c.3793G>C
|
ENSP00000245907.4:p.Gly1265Arg
|
|
ENST00000596238.1:n.236G>C
|
|
|
ENST00000601008.1:c.241+605G>C
|
ENSP00000471384.1:n.241+605G>C
|
|
NM_000064.3:c.3793G>C
|
NP_000055.2:p.Gly1265Arg
|
|
NM_000064.4:c.3793G>C
MANE Select
|
NP_000055.2:p.Gly1265Arg
|
|