ENST00000262367.10:c.7283G>C
MANE Select
|
ENSP00000262367.5:p.Gly2428Ala
|
|
ENST00000262367.9:c.7283G>C
|
ENSP00000262367.5:p.Gly2428Ala
|
|
ENST00000382070.7:c.7169G>C
|
ENSP00000371502.3:p.Gly2390Ala
|
|
NM_001079846.1:c.7169G>C
|
NP_001073315.1:p.Gly2390Ala
|
|
NM_004380.2:c.7283G>C
|
NP_004371.2:p.Gly2428Ala
|
|
XM_005255124.3:c.7238G>C
|
XP_005255181.1:p.Gly2413Ala
|
|
XM_005255125.3:c.6866G>C
|
XP_005255182.1:p.Gly2289Ala
|
|
XM_006720848.2:c.7022G>C
|
XP_006720911.1:p.Gly2341Ala
|
|
XM_011522380.1:c.7229G>C
|
XP_011520682.1:p.Gly2410Ala
|
|
XM_011522381.1:c.6530G>C
|
XP_011520683.1:p.Gly2177Ala
|
|
XM_005255124.4:c.7238G>C
|
XP_005255181.1:p.Gly2413Ala
|
|
XM_005255125.4:c.6866G>C
|
XP_005255182.1:p.Gly2289Ala
|
|
XM_006720848.3:c.7022G>C
|
XP_006720911.1:p.Gly2341Ala
|
|
XM_011522381.2:c.6530G>C
|
XP_011520683.1:p.Gly2177Ala
|
|
XM_017022944.1:c.7277G>C
|
XP_016878433.1:p.Gly2426Ala
|
|
NM_004380.3:c.7283G>C
MANE Select
|
NP_004371.2:p.Gly2428Ala
|
|