ENST00000304895.9:c.1856C>T
MANE Select
|
ENSP00000302728.4:p.Ala619Val
|
|
ENST00000304895.8:c.1856C>T
|
ENSP00000302728.4:p.Ala619Val
|
|
ENST00000421103.5:c.1418C>T
|
ENSP00000391390.1:p.Ala473Val
|
|
ENST00000430730.5:c.*1123C>T
|
ENSP00000411859.1:n.*1123C>T
|
|
ENST00000447929.5:c.*1236C>T
|
ENSP00000411262.1:n.*1236C>T
|
|
ENST00000466883.5:n.2246C>T
|
|
|
NM_000181.3:c.1856C>T
|
NP_000172.2:p.Ala619Val
|
|
NM_001284290.1:c.1418C>T
|
NP_001271219.1:p.Ala473Val
|
|
NM_001293104.1:c.1286C>T
|
NP_001280033.1:p.Ala429Val
|
|
NM_001293105.1:c.1199C>T
|
NP_001280034.1:p.Ala400Val
|
|
NR_120531.1:n.1902C>T
|
|
|
XM_005250297.3:c.1703C>T
|
XP_005250354.1:p.Ala568Val
|
|
XM_011516113.1:c.1355C>T
|
XP_011514415.1:p.Ala452Val
|
|
XM_011516114.1:c.1184C>T
|
XP_011514416.1:p.Ala395Val
|
|
XM_005250297.4:c.1703C>T
|
XP_005250354.1:p.Ala568Val
|
|
XM_011516114.2:c.1184C>T
|
XP_011514416.1:p.Ala395Val
|
|
XM_017012091.1:c.1202C>T
|
XP_016867580.1:p.Ala401Val
|
|
XM_017012092.1:c.1133C>T
|
XP_016867581.1:p.Ala378Val
|
|
XM_017012093.2:c.1031C>T
|
XP_016867582.1:p.Ala344Val
|
|
XR_001744658.2:n.1663C>T
|
|
|
XR_001744659.2:n.1776C>T
|
|
|
XR_001744660.2:n.1708C>T
|
|
|
XR_001744661.2:n.1623C>T
|
|
|
XR_927461.3:n.1861C>T
|
|
|
NM_000181.4:c.1856C>T
MANE Select
|
NP_000172.2:p.Ala619Val
|
|
NM_001284290.2:c.1418C>T
|
NP_001271219.1:p.Ala473Val
|
|
NM_001293104.2:c.1286C>T
|
NP_001280033.1:p.Ala429Val
|
|
NM_001293105.2:c.1199C>T
|
NP_001280034.1:p.Ala400Val
|
|
NR_120531.2:n.1801C>T
|
|
|