ENST00000682285.1:n.1186T>G
|
|
|
ENST00000682524.1:n.1186T>G
|
|
|
ENST00000683738.1:n.1186T>G
|
|
|
ENST00000355667.11:c.998T>G
|
ENSP00000347890.6:p.Val333Gly
|
|
ENST00000389253.9:c.998T>G
MANE Select
|
ENSP00000373905.4:p.Val333Gly
|
|
ENST00000355667.10:c.998T>G
|
ENSP00000347890.6:p.Val333Gly
|
|
ENST00000359692.10:c.998T>G
|
ENSP00000352721.6:p.Val333Gly
|
|
ENST00000389253.8:c.998T>G
|
ENSP00000373905.3:p.Val333Gly
|
|
ENST00000408974.8:c.998T>G
|
ENSP00000386192.3:p.Val333Gly
|
|
ENST00000585892.5:c.998T>G
|
ENSP00000468734.1:p.Val333Gly
|
|
ENST00000587485.1:n.504T>G
|
|
|
ENST00000587830.2:c.254T>G
|
ENSP00000466603.2:p.Val85Gly
|
|
ENST00000591701.5:n.358T>G
|
|
|
NM_001005360.2:c.998T>G
|
NP_001005360.1:p.Val333Gly
|
|
NM_001005361.2:c.998T>G
|
NP_001005361.1:p.Val333Gly
|
|
NM_001005362.2:c.998T>G
|
NP_001005362.1:p.Val333Gly
|
|
NM_001190716.1:c.998T>G
|
NP_001177645.1:p.Val333Gly
|
|
NM_004945.3:c.998T>G
|
NP_004936.2:p.Val333Gly
|
|
NM_001005361.3:c.998T>G
MANE Select
|
NP_001005361.1:p.Val333Gly
|
|
NM_001190716.2:c.998T>G
|
NP_001177645.1:p.Val333Gly
|
|
NM_001005360.3:c.998T>G
|
NP_001005360.1:p.Val333Gly
|
|
NM_001005362.3:c.998T>G
|
NP_001005362.1:p.Val333Gly
|
|
NM_004945.4:c.998T>G
|
NP_004936.2:p.Val333Gly
|
|