|
NM_016604.4:c.423G>A
MANE Select
|
NP_057688.3:p.Leu141=
|
|
ENST00000314358.10:c.423G>A
MANE Select
|
ENSP00000326563.5:p.Leu141=
|
|
NM_016604.3:c.423G>A
|
NP_057688.2:p.Leu141=
|
|
ENST00000314358.9:c.423G>A
|
ENSP00000326563.5:p.Leu141=
|
|
ENST00000510866.5:c.231G>A
|
ENSP00000425186.1:p.Leu77=
|
|
ENST00000512928.1:n.112G>A
|
|
|
XM_005272018.3:c.423G>A
|
XP_005272075.1:p.Leu141=
|
|
XM_005272018.4:c.423G>A
|
XP_005272075.1:p.Leu141=
|
|
XM_011543488.1:c.291G>A
|
XP_011541790.1:p.Leu97=
|
|
XM_011543488.2:c.291G>A
|
XP_011541790.1:p.Leu97=
|
|
XM_011543489.1:c.279G>A
|
XP_011541791.1:p.Leu93=
|
|
XM_011543489.2:c.279G>A
|
XP_011541791.1:p.Leu93=
|
|
XM_024446115.1:c.-52G>A
|
XP_024301883.1:n.-52G>A
|