ENST00000234071.8:c.139C>G
MANE Select
|
ENSP00000234071.4:p.Leu47Val
|
|
ENST00000234071.7:c.139C>G
|
ENSP00000234071.3:p.Leu47Val
|
|
ENST00000409048.1:c.139C>G
|
ENSP00000386679.1:p.Leu47Val
|
|
ENST00000419985.5:c.104C>G
|
ENSP00000392606.1:p.Pro35Arg
|
|
ENST00000427769.5:c.139C>G
|
ENSP00000406295.1:p.Leu47Val
|
|
ENST00000429925.5:c.139C>G
|
ENSP00000412697.1:p.Leu47Val
|
|
ENST00000431364.1:c.104C>G
|
ENSP00000391220.1:p.Pro35Arg
|
|
ENST00000442644.5:c.139C>G
|
ENSP00000411241.1:p.Leu47Val
|
|
ENST00000474030.5:n.222C>G
|
|
|
NM_000312.3:c.139C>G , LRG_599t1:c.139C>G
|
NP_000303.1:p.Leu47Val
|
|
XM_005263715.3:c.322C>G
|
XP_005263772.1:p.Leu108Val
|
|
XM_005263716.3:c.202C>G
|
XP_005263773.1:p.Leu68Val
|
|
XM_005263717.3:c.202C>G
|
XP_005263774.1:p.Leu68Val
|
|
XM_005263717.4:c.202C>G
|
XP_005263774.1:p.Leu68Val
|
|
XM_017004505.1:c.382C>G
|
XP_016859994.1:p.Leu128Val
|
|
XM_024453002.1:c.382C>G
|
XP_024308770.1:p.Leu128Val
|
|
XM_024453003.1:c.322C>G
|
XP_024308771.1:p.Leu108Val
|
|
XM_024453004.1:c.322C>G
|
XP_024308772.1:p.Leu108Val
|
|
XM_024453005.1:c.202C>G
|
XP_024308773.1:p.Leu68Val
|
|
XM_024453006.1:c.139C>G
|
XP_024308774.1:p.Leu47Val
|
|
NM_000312.4:c.139C>G
MANE Select
|
NP_000303.1:p.Leu47Val
|
|
NM_001375602.1:c.322C>G
|
NP_001362531.1:p.Leu108Val
|
|
NM_001375603.1:c.202C>G
|
NP_001362532.1:p.Leu68Val
|
|
NM_001375604.1:c.202C>G
|
NP_001362533.1:p.Leu68Val
|
|
NM_001375605.1:c.139C>G
|
NP_001362534.1:p.Leu47Val
|
|
NM_001375606.1:c.202C>G
|
NP_001362535.1:p.Leu68Val
|
|
NM_001375607.1:c.223C>G
|
NP_001362536.1:p.Leu75Val
|
|
NM_001375608.1:c.139C>G
|
NP_001362537.1:p.Leu47Val
|
|
NM_001375609.1:c.115C>G
|
NP_001362538.1:p.Leu39Val
|
|
NM_001375610.1:c.133C>G
|
NP_001362539.1:p.Leu45Val
|
|
NM_001375611.1:c.139C>G
|
NP_001362540.1:p.Leu47Val
|
|
NM_001375613.1:c.139C>G
|
NP_001362542.1:p.Leu47Val
|
|