|
ENST00000304895.9:c.145G>T
MANE Select
|
ENSP00000302728.4:p.Ala49Ser
|
|
|
ENST00000304895.8:c.145G>T
|
ENSP00000302728.4:p.Ala49Ser
|
|
|
ENST00000421103.5:c.145G>T
|
ENSP00000391390.1:p.Ala49Ser
|
|
|
ENST00000430730.5:c.145G>T
|
ENSP00000411859.1:p.Ala49Ser
|
|
|
ENST00000446111.1:c.145G>T
|
ENSP00000416793.1:p.Ala49Ser
|
|
|
ENST00000447929.5:c.145G>T
|
ENSP00000411262.1:p.Ala49Ser
|
|
|
ENST00000475316.5:n.50G>T
|
|
|
|
NM_000181.3:c.145G>T
|
NP_000172.2:p.Ala49Ser
|
|
|
NM_001284290.1:c.145G>T
|
NP_001271219.1:p.Ala49Ser
|
|
|
NM_001293104.1:c.-241G>T
|
NP_001280033.1:n.-241G>T
|
|
|
NM_001293105.1:c.-185G>T
|
NP_001280034.1:n.-185G>T
|
|
|
NR_120531.1:n.276G>T
|
|
|
|
XM_005250297.3:c.145G>T
|
XP_005250354.1:p.Ala49Ser
|
|
|
XM_011516113.1:c.-185G>T
|
XP_011514415.1:n.-185G>T
|
|
|
XR_927461.1:n.271G>T
|
|
|
|
XM_005250297.4:c.145G>T
|
XP_005250354.1:p.Ala49Ser
|
|
|
XM_011516114.2:c.-541G>T
|
XP_011514416.1:n.-541G>T
|
|
|
XM_017012091.1:c.-185G>T
|
XP_016867580.1:n.-185G>T
|
|
|
XM_017012092.1:c.-241G>T
|
XP_016867581.1:n.-241G>T
|
|
|
XM_017012093.2:c.-541G>T
|
XP_016867582.1:n.-541G>T
|
|
|
XR_001744658.2:n.190G>T
|
|
|
|
XR_001744659.2:n.190G>T
|
|
|
|
XR_001744660.2:n.190G>T
|
|
|
|
XR_001744661.2:n.190G>T
|
|
|
|
XR_927461.3:n.190G>T
|
|
|
|
NM_000181.4:c.145G>T
MANE Select
|
NP_000172.2:p.Ala49Ser
|
|
|
NM_001284290.2:c.145G>T
|
NP_001271219.1:p.Ala49Ser
|
|
|
NM_001293104.2:c.-241G>T
|
NP_001280033.1:n.-241G>T
|
|
|
NM_001293105.2:c.-185G>T
|
NP_001280034.1:n.-185G>T
|
|
|
NR_120531.2:n.175G>T
|
|
|
