ENST00000262367.10:c.7102C>T
MANE Select
|
ENSP00000262367.5:p.Gln2368Ter
|
|
ENST00000262367.9:c.7102C>T
|
ENSP00000262367.5:p.Gln2368Ter
|
|
ENST00000382070.7:c.6988C>T
|
ENSP00000371502.3:p.Gln2330Ter
|
|
NM_001079846.1:c.6988C>T
|
NP_001073315.1:p.Gln2330Ter
|
|
NM_004380.2:c.7102C>T
|
NP_004371.2:p.Gln2368Ter
|
|
XM_005255124.3:c.7057C>T
|
XP_005255181.1:p.Gln2353Ter
|
|
XM_005255125.3:c.6685C>T
|
XP_005255182.1:p.Gln2229Ter
|
|
XM_006720848.2:c.6841C>T
|
XP_006720911.1:p.Gln2281Ter
|
|
XM_011522380.1:c.7048C>T
|
XP_011520682.1:p.Gln2350Ter
|
|
XM_011522381.1:c.6349C>T
|
XP_011520683.1:p.Gln2117Ter
|
|
XM_005255124.4:c.7057C>T
|
XP_005255181.1:p.Gln2353Ter
|
|
XM_005255125.4:c.6685C>T
|
XP_005255182.1:p.Gln2229Ter
|
|
XM_006720848.3:c.6841C>T
|
XP_006720911.1:p.Gln2281Ter
|
|
XM_011522381.2:c.6349C>T
|
XP_011520683.1:p.Gln2117Ter
|
|
XM_017022944.1:c.7096C>T
|
XP_016878433.1:p.Gln2366Ter
|
|
NM_004380.3:c.7102C>T
MANE Select
|
NP_004371.2:p.Gln2368Ter
|
|