ENST00000449082.3:c.3121G>C
MANE Select
|
ENSP00000390600.2:p.Asp1041His
|
|
ENST00000643924.1:c.3118G>C
|
ENSP00000495595.1:p.Asp1040His
|
|
ENST00000655275.1:c.3145G>C
|
ENSP00000499510.1:p.Asp1049His
|
|
ENST00000449082.2:c.3121G>C
|
ENSP00000390600.2:p.Asp1041His
|
|
NM_001293306.2:c.3118G>C
|
NP_001280235.2:p.Asp1040His
|
|
NM_001293307.2:c.2827G>C
|
NP_001280236.2:p.Asp943His
|
|
NM_006514.3:c.3121G>C
|
NP_006505.3:p.Asp1041His
|
|
XM_005265371.2:c.3130G>C
|
XP_005265428.1:p.Asp1044His
|
|
XM_011533993.1:c.3127G>C
|
XP_011532295.1:p.Asp1043His
|
|
XM_011533994.1:c.2836G>C
|
XP_011532296.1:p.Asp946His
|
|
XM_005265371.3:c.3130G>C
|
XP_005265428.1:p.Asp1044His
|
|
XM_011533993.2:c.3127G>C
|
XP_011532295.1:p.Asp1043His
|
|
XM_011533994.2:c.2836G>C
|
XP_011532296.1:p.Asp946His
|
|
NM_006514.4:c.3121G>C
MANE Select
|
NP_006505.4:p.Asp1041His
|
|