ENST00000304895.9:c.69G>T
MANE Select
|
ENSP00000302728.4:p.Leu23=
|
|
ENST00000304895.8:c.69G>T
|
ENSP00000302728.4:p.Leu23=
|
|
ENST00000421103.5:c.69G>T
|
ENSP00000391390.1:p.Leu23=
|
|
ENST00000430730.5:c.69G>T
|
ENSP00000411859.1:p.Leu23=
|
|
ENST00000446111.1:c.69G>T
|
ENSP00000416793.1:p.Leu23=
|
|
ENST00000447929.5:c.69G>T
|
ENSP00000411262.1:p.Leu23=
|
|
NM_000181.3:c.69G>T
|
NP_000172.2:p.Leu23=
|
|
NM_001284290.1:c.69G>T
|
NP_001271219.1:p.Leu23=
|
|
NM_001293104.1:c.-317G>T
|
NP_001280033.1:n.-317G>T
|
|
NM_001293105.1:c.-261G>T
|
NP_001280034.1:n.-261G>T
|
|
NR_120531.1:n.200G>T
|
|
|
XM_005250297.3:c.69G>T
|
XP_005250354.1:p.Leu23=
|
|
XM_011516113.1:c.-261G>T
|
XP_011514415.1:n.-261G>T
|
|
XR_927461.1:n.195G>T
|
|
|
XM_005250297.4:c.69G>T
|
XP_005250354.1:p.Leu23=
|
|
XM_011516114.2:c.-617G>T
|
XP_011514416.1:n.-617G>T
|
|
XM_017012091.1:c.-261G>T
|
XP_016867580.1:n.-261G>T
|
|
XM_017012092.1:c.-317G>T
|
XP_016867581.1:n.-317G>T
|
|
XM_017012093.2:c.-617G>T
|
XP_016867582.1:n.-617G>T
|
|
XR_001744658.2:n.114G>T
|
|
|
XR_001744659.2:n.114G>T
|
|
|
XR_001744660.2:n.114G>T
|
|
|
XR_001744661.2:n.114G>T
|
|
|
XR_927461.3:n.114G>T
|
|
|
NM_000181.4:c.69G>T
MANE Select
|
NP_000172.2:p.Leu23=
|
|
NM_001284290.2:c.69G>T
|
NP_001271219.1:p.Leu23=
|
|
NM_001293104.2:c.-317G>T
|
NP_001280033.1:n.-317G>T
|
|
NM_001293105.2:c.-261G>T
|
NP_001280034.1:n.-261G>T
|
|
NR_120531.2:n.99G>T
|
|
|