ENST00000262367.10:c.6912G>T
MANE Select
|
ENSP00000262367.5:p.Gln2304His
|
|
ENST00000262367.9:c.6912G>T
|
ENSP00000262367.5:p.Gln2304His
|
|
ENST00000382070.7:c.6798G>T
|
ENSP00000371502.3:p.Gln2266His
|
|
NM_001079846.1:c.6798G>T
|
NP_001073315.1:p.Gln2266His
|
|
NM_004380.2:c.6912G>T
|
NP_004371.2:p.Gln2304His
|
|
XM_005255124.3:c.6867G>T
|
XP_005255181.1:p.Gln2289His
|
|
XM_005255125.3:c.6495G>T
|
XP_005255182.1:p.Gln2165His
|
|
XM_006720848.2:c.6651G>T
|
XP_006720911.1:p.Gln2217His
|
|
XM_011522380.1:c.6858G>T
|
XP_011520682.1:p.Gln2286His
|
|
XM_011522381.1:c.6159G>T
|
XP_011520683.1:p.Gln2053His
|
|
XM_005255124.4:c.6867G>T
|
XP_005255181.1:p.Gln2289His
|
|
XM_005255125.4:c.6495G>T
|
XP_005255182.1:p.Gln2165His
|
|
XM_006720848.3:c.6651G>T
|
XP_006720911.1:p.Gln2217His
|
|
XM_011522381.2:c.6159G>T
|
XP_011520683.1:p.Gln2053His
|
|
XM_017022944.1:c.6906G>T
|
XP_016878433.1:p.Gln2302His
|
|
NM_004380.3:c.6912G>T
MANE Select
|
NP_004371.2:p.Gln2304His
|
|