ENST00000256084.8:c.3049G=
MANE Select
|
ENSP00000256084.7:p.Asp1017=
|
|
ENST00000256084.7:c.3049G=
|
ENSP00000256084.7:p.Asp1017=
|
|
ENST00000359874.7:c.3139G=
|
ENSP00000352936.3:p.Asp1047=
|
|
NM_001127698.1:c.3139G=
|
NP_001121170.1:p.Asp1047=
|
|
NM_006846.3:c.3049G= , LRG_110t1:c.3049G=
|
NP_006837.2:p.Asp1017=
|
|
XM_011537550.1:c.3082G=
|
XP_011535852.1:p.Asp1028=
|
|
XM_011537551.1:c.3055G=
|
XP_011535853.1:p.Asp1019=
|
|
XM_011537551.2:c.3055G=
|
XP_011535853.1:p.Asp1019=
|
|
NM_001127698.2:c.3139G=
|
NP_001121170.1:p.Asp1047=
|
|
NM_006846.4:c.3049G=
MANE Select
|
NP_006837.2:p.Asp1017=
|
|