ENST00000262367.10:c.7104G>C
MANE Select
|
ENSP00000262367.5:p.Gln2368His
|
|
ENST00000262367.9:c.7104G>C
|
ENSP00000262367.5:p.Gln2368His
|
|
ENST00000382070.7:c.6990G>C
|
ENSP00000371502.3:p.Gln2330His
|
|
NM_001079846.1:c.6990G>C
|
NP_001073315.1:p.Gln2330His
|
|
NM_004380.2:c.7104G>C
|
NP_004371.2:p.Gln2368His
|
|
XM_005255124.3:c.7059G>C
|
XP_005255181.1:p.Gln2353His
|
|
XM_005255125.3:c.6687G>C
|
XP_005255182.1:p.Gln2229His
|
|
XM_006720848.2:c.6843G>C
|
XP_006720911.1:p.Gln2281His
|
|
XM_011522380.1:c.7050G>C
|
XP_011520682.1:p.Gln2350His
|
|
XM_011522381.1:c.6351G>C
|
XP_011520683.1:p.Gln2117His
|
|
XM_005255124.4:c.7059G>C
|
XP_005255181.1:p.Gln2353His
|
|
XM_005255125.4:c.6687G>C
|
XP_005255182.1:p.Gln2229His
|
|
XM_006720848.3:c.6843G>C
|
XP_006720911.1:p.Gln2281His
|
|
XM_011522381.2:c.6351G>C
|
XP_011520683.1:p.Gln2117His
|
|
XM_017022944.1:c.7098G>C
|
XP_016878433.1:p.Gln2366His
|
|
NM_004380.3:c.7104G>C
MANE Select
|
NP_004371.2:p.Gln2368His
|
|