ENST00000324288.14:c.2664C>T
MANE Select
|
ENSP00000316328.8:p.Ala888=
|
|
ENST00000324288.12:c.2664C>T
|
ENSP00000316328.8:p.Ala888=
|
|
ENST00000381835.9:c.912C>T
|
ENSP00000371257.5:p.Ala304=
|
|
ENST00000537380.1:n.1007-1153C>T
|
|
|
ENST00000570546.5:n.3664C>T
|
|
|
ENST00000618207.4:c.1007-1153C>T
|
ENSP00000484761.1:n.1007-1153C>T
|
|
ENST00000618327.4:c.2667C>T
|
ENSP00000485010.1:p.Ala889=
|
|
NM_000246.3:c.2664C>T , LRG_49t1:c.2664C>T
|
NP_000237.2:p.Ala888=
|
|
NM_001286402.1:c.2667C>T
|
NP_001273331.1:p.Ala889=
|
|
NM_001286403.1:c.912C>T
|
NP_001273332.1:p.Ala304=
|
|
NR_104444.1:n.1140-1153C>T
|
|
|
XM_006720880.2:c.2961C>T
|
XP_006720943.2:p.Ala987=
|
|
XM_011522484.1:c.2961C>T
|
XP_011520786.1:p.Ala987=
|
|
XM_011522485.1:c.2961C>T
|
XP_011520787.1:p.Ala987=
|
|
XM_011522486.1:c.2961C>T
|
XP_011520788.1:p.Ala987=
|
|
XM_011522487.1:c.2715C>T
|
XP_011520789.1:p.Ala905=
|
|
XM_011522488.1:c.2712C>T
|
XP_011520790.1:p.Ala904=
|
|
XM_011522489.1:c.2712C>T
|
XP_011520791.1:p.Ala904=
|
|
XM_011522490.1:c.2709C>T
|
XP_011520792.1:p.Ala903=
|
|
XM_011522491.1:c.2961C>T
|
XP_011520793.1:p.Ala987=
|
|
XM_011522492.1:c.2667C>T
|
XP_011520794.1:p.Ala889=
|
|
XM_011522493.1:c.2664C>T
|
XP_011520795.1:p.Ala888=
|
|
XM_011522494.1:c.2595C>T
|
XP_011520796.1:p.Ala865=
|
|
XM_011522495.1:c.2520C>T
|
XP_011520797.1:p.Ala840=
|
|
XM_011522496.1:c.2517C>T
|
XP_011520798.1:p.Ala839=
|
|
XR_932841.1:n.2976C>T
|
|
|
XR_932842.1:n.2976C>T
|
|
|
XR_932843.1:n.2976C>T
|
|
|
XR_932846.1:n.3022C>T
|
|
|
XR_932847.1:n.3022C>T
|
|
|
XR_932848.1:n.1062C>T
|
|
|
XM_006720880.3:c.2961C>T
|
XP_006720943.2:p.Ala987=
|
|
XM_011522484.3:c.2961C>T
|
XP_011520786.1:p.Ala987=
|
|
XM_011522485.2:c.2961C>T
|
XP_011520787.1:p.Ala987=
|
|
XM_011522486.2:c.2961C>T
|
XP_011520788.1:p.Ala987=
|
|
XM_011522487.2:c.2715C>T
|
XP_011520789.1:p.Ala905=
|
|
XM_011522488.2:c.2712C>T
|
XP_011520790.1:p.Ala904=
|
|
XM_011522489.2:c.2712C>T
|
XP_011520791.1:p.Ala904=
|
|
XM_011522490.2:c.2709C>T
|
XP_011520792.1:p.Ala903=
|
|
XM_011522491.2:c.2961C>T
|
XP_011520793.1:p.Ala987=
|
|
XM_011522492.2:c.2667C>T
|
XP_011520794.1:p.Ala889=
|
|
XM_011522493.2:c.2664C>T
|
XP_011520795.1:p.Ala888=
|
|
XM_011522494.2:c.2595C>T
|
XP_011520796.1:p.Ala865=
|
|
XM_011522495.2:c.2520C>T
|
XP_011520797.1:p.Ala840=
|
|
XM_011522496.2:c.2517C>T
|
XP_011520798.1:p.Ala839=
|
|
XM_024450280.1:c.2907C>T
|
XP_024306048.1:p.Ala969=
|
|
XM_024450281.1:c.2760C>T
|
XP_024306049.1:p.Ala920=
|
|
XR_001751904.1:n.3026C>T
|
|
|
XR_932841.3:n.2978C>T
|
|
|
XR_932842.2:n.2978C>T
|
|
|
XR_932846.3:n.3026C>T
|
|
|
XR_932847.3:n.3026C>T
|
|
|
NM_001286403.2:c.912C>T
|
NP_001273332.1:p.Ala304=
|
|
NR_104444.2:n.1136-1153C>T
|
|
|
NM_000246.4:c.2664C>T
MANE Select
|
NP_000237.2:p.Ala888=
|
|
NM_001379330.1:c.2520C>T
|
NP_001366259.1:p.Ala840=
|
|
NM_001379331.1:c.2517C>T
|
NP_001366260.1:p.Ala839=
|
|
NM_001379332.1:c.2667C>T
|
NP_001366261.1:p.Ala889=
|
|
NM_001379333.1:c.2664C>T
|
NP_001366262.1:p.Ala888=
|
|
NM_001379334.1:c.2595C>T
|
NP_001366263.1:p.Ala865=
|
|