ENST00000396128.9:c.949C=
MANE Select
|
ENSP00000379434.4:p.Leu317=
|
|
ENST00000355081.3:c.991C=
|
ENSP00000347193.2:p.Leu331=
|
|
ENST00000396128.8:c.949C=
|
ENSP00000379434.3:p.Leu317=
|
|
NM_001308112.1:c.991C=
|
NP_001295041.1:p.Leu331=
|
|
NM_017658.3:c.949C=
|
NP_060128.2:p.Leu317=
|
|
NM_017658.4:c.949C=
|
NP_060128.2:p.Leu317=
|
|
XM_005267770.2:c.949C=
|
XP_005267827.1:p.Leu317=
|
|
XM_011536847.1:c.949C=
|
XP_011535149.1:p.Leu317=
|
|
XM_011536848.1:c.949C=
|
XP_011535150.1:p.Leu317=
|
|
XM_011536849.1:c.991C=
|
XP_011535151.1:p.Leu331=
|
|
XM_005267770.4:c.949C=
|
XP_005267827.1:p.Leu317=
|
|
XM_011536847.3:c.949C=
|
XP_011535149.1:p.Leu317=
|
|
XM_011536849.2:c.991C=
|
XP_011535151.1:p.Leu331=
|
|
XM_024449635.1:c.949C=
|
XP_024305403.1:p.Leu317=
|
|
NM_001308112.2:c.991C=
|
NP_001295041.1:p.Leu331=
|
|
NM_017658.5:c.949C=
MANE Select
|
NP_060128.2:p.Leu317=
|
|