ENST00000304895.9:c.1935G>C
MANE Select
|
ENSP00000302728.4:p.Leu645Phe
|
|
ENST00000304895.8:c.1935G>C
|
ENSP00000302728.4:p.Leu645Phe
|
|
ENST00000421103.5:c.1497G>C
|
ENSP00000391390.1:p.Leu499Phe
|
|
ENST00000430730.5:c.*1202G>C
|
ENSP00000411859.1:n.*1202G>C
|
|
ENST00000447929.5:c.*1315G>C
|
ENSP00000411262.1:n.*1315G>C
|
|
ENST00000466883.5:n.2325G>C
|
|
|
NM_000181.3:c.1935G>C
|
NP_000172.2:p.Leu645Phe
|
|
NM_001284290.1:c.1497G>C
|
NP_001271219.1:p.Leu499Phe
|
|
NM_001293104.1:c.1365G>C
|
NP_001280033.1:p.Leu455Phe
|
|
NM_001293105.1:c.1278G>C
|
NP_001280034.1:p.Leu426Phe
|
|
NR_120531.1:n.1981G>C
|
|
|
XM_005250297.3:c.1782G>C
|
XP_005250354.1:p.Leu594Phe
|
|
XM_011516113.1:c.1434G>C
|
XP_011514415.1:p.Leu478Phe
|
|
XM_011516114.1:c.1263G>C
|
XP_011514416.1:p.Leu421Phe
|
|
XM_005250297.4:c.1782G>C
|
XP_005250354.1:p.Leu594Phe
|
|
XM_011516114.2:c.1263G>C
|
XP_011514416.1:p.Leu421Phe
|
|
XM_017012091.1:c.1281G>C
|
XP_016867580.1:p.Leu427Phe
|
|
XM_017012092.1:c.1212G>C
|
XP_016867581.1:p.Leu404Phe
|
|
XM_017012093.2:c.1110G>C
|
XP_016867582.1:p.Leu370Phe
|
|
XR_001744658.2:n.1742G>C
|
|
|
XR_001744659.2:n.1855G>C
|
|
|
XR_001744660.2:n.1787G>C
|
|
|
XR_001744661.2:n.1702G>C
|
|
|
XR_927461.3:n.1940G>C
|
|
|
NM_000181.4:c.1935G>C
MANE Select
|
NP_000172.2:p.Leu645Phe
|
|
NM_001284290.2:c.1497G>C
|
NP_001271219.1:p.Leu499Phe
|
|
NM_001293104.2:c.1365G>C
|
NP_001280033.1:p.Leu455Phe
|
|
NM_001293105.2:c.1278G>C
|
NP_001280034.1:p.Leu426Phe
|
|
NR_120531.2:n.1880G>C
|
|
|