ENST00000710359.1:c.7073G=
|
ENSP00000518230.1:p.Arg2358=
|
|
ENST00000379802.8:c.8402G=
MANE Select
|
ENSP00000369129.3:p.Arg2801=
|
|
ENST00000379802.7:c.8402G=
|
ENSP00000369129.3:p.Arg2801=
|
|
ENST00000418664.2:c.6605G=
|
ENSP00000396591.2:p.Arg2202=
|
|
NM_001008844.1:c.6605G=
|
NP_001008844.1:p.Arg2202=
|
|
NM_004415.2:c.8402G= , LRG_423t1:c.8402G=
|
NP_004406.2:p.Arg2801=
|
|
XM_011514323.1:c.7073G=
|
XP_011512625.1:p.Arg2358=
|
|
NM_001008844.2:c.6605G=
|
NP_001008844.1:p.Arg2202=
|
|
NM_001319034.1:c.7073G=
|
NP_001305963.1:p.Arg2358=
|
|
NM_004415.3:c.8402G=
|
NP_004406.2:p.Arg2801=
|
|
NM_004415.4:c.8402G=
MANE Select
|
NP_004406.2:p.Arg2801=
|
|
NM_001008844.3:c.6605G=
|
NP_001008844.1:p.Arg2202=
|
|
NM_001319034.2:c.7073G=
|
NP_001305963.1:p.Arg2358=
|
|