ENST00000274547.7:c.474T>G
|
ENSP00000274547.2:p.Ala158=
|
|
ENST00000393959.6:c.474T>G
MANE Select
|
ENSP00000377531.1:p.Ala158=
|
|
ENST00000674514.1:n.556T>G
|
|
|
ENST00000675081.1:c.222T>G
|
ENSP00000502207.1:p.Ala74=
|
|
ENST00000675303.1:c.474T>G
|
ENSP00000502748.1:p.Ala158=
|
|
ENST00000675381.1:c.222T>G
|
ENSP00000501968.1:p.Ala74=
|
|
ENST00000675773.1:c.474T>G
|
ENSP00000502701.1:p.Ala158=
|
|
ENST00000274547.6:c.474T>G
|
ENSP00000274547.2:p.Ala158=
|
|
ENST00000353437.10:c.474T>G
|
ENSP00000274546.6:p.Ala158=
|
|
ENST00000393959.5:c.474T>G
|
ENSP00000377531.1:p.Ala158=
|
|
ENST00000517547.5:c.-7T>G
|
ENSP00000429750.1:n.-7T>G
|
|
ENST00000517901.5:c.285T>G
|
ENSP00000430532.1:p.Ala95=
|
|
ENST00000520240.5:c.474T>G
|
ENSP00000429320.1:p.Ala158=
|
|
ENST00000612710.1:c.285T>G
|
ENSP00000480066.1:p.Ala95=
|
|
NM_000813.2:c.474T>G
|
NP_000804.1:p.Ala158=
|
|
NM_021911.2:c.474T>G
|
NP_068711.1:p.Ala158=
|
|
NM_000813.3:c.474T>G
|
NP_000804.1:p.Ala158=
|
|
NM_001371727.1:c.474T>G
MANE Select
|
NP_001358656.1:p.Ala158=
|
|
NM_021911.3:c.474T>G
|
NP_068711.1:p.Ala158=
|
|