ENST00000262367.10:c.7122C>A
MANE Select
|
ENSP00000262367.5:p.His2374Gln
|
|
ENST00000262367.9:c.7122C>A
|
ENSP00000262367.5:p.His2374Gln
|
|
ENST00000382070.7:c.7008C>A
|
ENSP00000371502.3:p.His2336Gln
|
|
NM_001079846.1:c.7008C>A
|
NP_001073315.1:p.His2336Gln
|
|
NM_004380.2:c.7122C>A
|
NP_004371.2:p.His2374Gln
|
|
XM_005255124.3:c.7077C>A
|
XP_005255181.1:p.His2359Gln
|
|
XM_005255125.3:c.6705C>A
|
XP_005255182.1:p.His2235Gln
|
|
XM_006720848.2:c.6861C>A
|
XP_006720911.1:p.His2287Gln
|
|
XM_011522380.1:c.7068C>A
|
XP_011520682.1:p.His2356Gln
|
|
XM_011522381.1:c.6369C>A
|
XP_011520683.1:p.His2123Gln
|
|
XM_005255124.4:c.7077C>A
|
XP_005255181.1:p.His2359Gln
|
|
XM_005255125.4:c.6705C>A
|
XP_005255182.1:p.His2235Gln
|
|
XM_006720848.3:c.6861C>A
|
XP_006720911.1:p.His2287Gln
|
|
XM_011522381.2:c.6369C>A
|
XP_011520683.1:p.His2123Gln
|
|
XM_017022944.1:c.7116C>A
|
XP_016878433.1:p.His2372Gln
|
|
NM_004380.3:c.7122C>A
MANE Select
|
NP_004371.2:p.His2374Gln
|
|