ENST00000695651.1:n.2136G>A
|
|
|
ENST00000695652.1:c.3665G>A
|
ENSP00000512083.1:p.Gly1222Asp
|
|
ENST00000695653.1:c.1697G>A
|
ENSP00000512084.1:p.Gly566Asp
|
|
ENST00000695654.1:c.2813G>A
|
ENSP00000512085.1:p.Gly938Asp
|
|
ENST00000695655.1:c.2729G>A
|
ENSP00000512086.1:n.2729G>A
|
|
ENST00000695692.1:n.3152G>A
|
|
|
ENST00000245907.11:c.3788G>A
MANE Select
|
ENSP00000245907.4:p.Gly1263Asp
|
|
ENST00000245907.10:c.3788G>A
|
ENSP00000245907.4:p.Gly1263Asp
|
|
ENST00000596238.1:n.231G>A
|
|
|
ENST00000601008.1:c.241+600G>A
|
ENSP00000471384.1:n.241+600G>A
|
|
NM_000064.3:c.3788G>A
|
NP_000055.2:p.Gly1263Asp
|
|
NM_000064.4:c.3788G>A
MANE Select
|
NP_000055.2:p.Gly1263Asp
|
|