ENST00000262367.10:c.7102C=
MANE Select
|
ENSP00000262367.5:p.Gln2368=
|
|
ENST00000262367.9:c.7102C=
|
ENSP00000262367.5:p.Gln2368=
|
|
ENST00000382070.7:c.6988C=
|
ENSP00000371502.3:p.Gln2330=
|
|
NM_001079846.1:c.6988C=
|
NP_001073315.1:p.Gln2330=
|
|
NM_004380.2:c.7102C=
|
NP_004371.2:p.Gln2368=
|
|
XM_005255124.3:c.7057C=
|
XP_005255181.1:p.Gln2353=
|
|
XM_005255125.3:c.6685C=
|
XP_005255182.1:p.Gln2229=
|
|
XM_006720848.2:c.6841C=
|
XP_006720911.1:p.Gln2281=
|
|
XM_011522380.1:c.7048C=
|
XP_011520682.1:p.Gln2350=
|
|
XM_011522381.1:c.6349C=
|
XP_011520683.1:p.Gln2117=
|
|
XM_005255124.4:c.7057C=
|
XP_005255181.1:p.Gln2353=
|
|
XM_005255125.4:c.6685C=
|
XP_005255182.1:p.Gln2229=
|
|
XM_006720848.3:c.6841C=
|
XP_006720911.1:p.Gln2281=
|
|
XM_011522381.2:c.6349C=
|
XP_011520683.1:p.Gln2117=
|
|
XM_017022944.1:c.7096C=
|
XP_016878433.1:p.Gln2366=
|
|
NM_004380.3:c.7102C=
MANE Select
|
NP_004371.2:p.Gln2368=
|
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