ENST00000262367.10:c.6198T>C
MANE Select
|
ENSP00000262367.5:p.Ala2066=
|
|
ENST00000262367.9:c.6198T>C
|
ENSP00000262367.5:p.Ala2066=
|
|
ENST00000382070.7:c.6084T>C
|
ENSP00000371502.3:p.Ala2028=
|
|
NM_001079846.1:c.6084T>C
|
NP_001073315.1:p.Ala2028=
|
|
NM_004380.2:c.6198T>C
|
NP_004371.2:p.Ala2066=
|
|
XM_005255124.3:c.6153T>C
|
XP_005255181.1:p.Ala2051=
|
|
XM_005255125.3:c.5781T>C
|
XP_005255182.1:p.Ala1927=
|
|
XM_006720848.2:c.5937T>C
|
XP_006720911.1:p.Ala1979=
|
|
XM_011522380.1:c.6144T>C
|
XP_011520682.1:p.Ala2048=
|
|
XM_011522381.1:c.5445T>C
|
XP_011520683.1:p.Ala1815=
|
|
XM_005255124.4:c.6153T>C
|
XP_005255181.1:p.Ala2051=
|
|
XM_005255125.4:c.5781T>C
|
XP_005255182.1:p.Ala1927=
|
|
XM_006720848.3:c.5937T>C
|
XP_006720911.1:p.Ala1979=
|
|
XM_011522381.2:c.5445T>C
|
XP_011520683.1:p.Ala1815=
|
|
XM_017022944.1:c.6192T>C
|
XP_016878433.1:p.Ala2064=
|
|
NM_004380.3:c.6198T>C
MANE Select
|
NP_004371.2:p.Ala2066=
|
|