ENST00000304895.9:c.1819G>T
MANE Select
|
ENSP00000302728.4:p.Gly607Trp
|
|
ENST00000304895.8:c.1819G>T
|
ENSP00000302728.4:p.Gly607Trp
|
|
ENST00000421103.5:c.1381G>T
|
ENSP00000391390.1:p.Gly461Trp
|
|
ENST00000430730.5:c.*1086G>T
|
ENSP00000411859.1:n.*1086G>T
|
|
ENST00000447929.5:c.*1199G>T
|
ENSP00000411262.1:n.*1199G>T
|
|
ENST00000466883.5:n.2209G>T
|
|
|
NM_000181.3:c.1819G>T
|
NP_000172.2:p.Gly607Trp
|
|
NM_001284290.1:c.1381G>T
|
NP_001271219.1:p.Gly461Trp
|
|
NM_001293104.1:c.1249G>T
|
NP_001280033.1:p.Gly417Trp
|
|
NM_001293105.1:c.1162G>T
|
NP_001280034.1:p.Gly388Trp
|
|
NR_120531.1:n.1865G>T
|
|
|
XM_005250297.3:c.1666G>T
|
XP_005250354.1:p.Gly556Trp
|
|
XM_011516113.1:c.1318G>T
|
XP_011514415.1:p.Gly440Trp
|
|
XM_011516114.1:c.1147G>T
|
XP_011514416.1:p.Gly383Trp
|
|
XM_005250297.4:c.1666G>T
|
XP_005250354.1:p.Gly556Trp
|
|
XM_011516114.2:c.1147G>T
|
XP_011514416.1:p.Gly383Trp
|
|
XM_017012091.1:c.1165G>T
|
XP_016867580.1:p.Gly389Trp
|
|
XM_017012092.1:c.1096G>T
|
XP_016867581.1:p.Gly366Trp
|
|
XM_017012093.2:c.994G>T
|
XP_016867582.1:p.Gly332Trp
|
|
XR_001744658.2:n.1626G>T
|
|
|
XR_001744659.2:n.1739G>T
|
|
|
XR_001744660.2:n.1671G>T
|
|
|
XR_001744661.2:n.1586G>T
|
|
|
XR_927461.3:n.1824G>T
|
|
|
NM_000181.4:c.1819G>T
MANE Select
|
NP_000172.2:p.Gly607Trp
|
|
NM_001284290.2:c.1381G>T
|
NP_001271219.1:p.Gly461Trp
|
|
NM_001293104.2:c.1249G>T
|
NP_001280033.1:p.Gly417Trp
|
|
NM_001293105.2:c.1162G>T
|
NP_001280034.1:p.Gly388Trp
|
|
NR_120531.2:n.1764G>T
|
|
|