ENST00000262367.10:c.6135G>C
MANE Select
|
ENSP00000262367.5:p.Gln2045His
|
|
ENST00000262367.9:c.6135G>C
|
ENSP00000262367.5:p.Gln2045His
|
|
ENST00000382070.7:c.6021G>C
|
ENSP00000371502.3:p.Gln2007His
|
|
NM_001079846.1:c.6021G>C
|
NP_001073315.1:p.Gln2007His
|
|
NM_004380.2:c.6135G>C
|
NP_004371.2:p.Gln2045His
|
|
XM_005255124.3:c.6090G>C
|
XP_005255181.1:p.Gln2030His
|
|
XM_005255125.3:c.5718G>C
|
XP_005255182.1:p.Gln1906His
|
|
XM_006720848.2:c.5874G>C
|
XP_006720911.1:p.Gln1958His
|
|
XM_011522380.1:c.6081G>C
|
XP_011520682.1:p.Gln2027His
|
|
XM_011522381.1:c.5382G>C
|
XP_011520683.1:p.Gln1794His
|
|
XM_005255124.4:c.6090G>C
|
XP_005255181.1:p.Gln2030His
|
|
XM_005255125.4:c.5718G>C
|
XP_005255182.1:p.Gln1906His
|
|
XM_006720848.3:c.5874G>C
|
XP_006720911.1:p.Gln1958His
|
|
XM_011522381.2:c.5382G>C
|
XP_011520683.1:p.Gln1794His
|
|
XM_017022944.1:c.6129G>C
|
XP_016878433.1:p.Gln2043His
|
|
NM_004380.3:c.6135G>C
MANE Select
|
NP_004371.2:p.Gln2045His
|
|