ENST00000234071.8:c.1231C>G
MANE Select
|
ENSP00000234071.4:p.His411Asp
|
|
ENST00000234071.7:c.1231C>G
|
ENSP00000234071.3:p.His411Asp
|
|
ENST00000402125.2:c.555C>G
|
|
|
ENST00000409048.1:c.1333C>G
|
ENSP00000386679.1:p.His445Asp
|
|
NM_000312.3:c.1231C>G , LRG_599t1:c.1231C>G
|
NP_000303.1:p.His411Asp
|
|
XM_005263715.3:c.1414C>G
|
XP_005263772.1:p.His472Asp
|
|
XM_005263716.3:c.1396C>G
|
XP_005263773.1:p.His466Asp
|
|
XM_005263717.3:c.1294C>G
|
XP_005263774.1:p.His432Asp
|
|
XR_923313.1:n.1332-527G>C
|
|
|
XM_005263717.4:c.1294C>G
|
XP_005263774.1:p.His432Asp
|
|
XM_017004505.1:c.1474C>G
|
XP_016859994.1:p.His492Asp
|
|
XM_024453002.1:c.1576C>G
|
XP_024308770.1:p.His526Asp
|
|
XM_024453003.1:c.1516C>G
|
XP_024308771.1:p.His506Asp
|
|
XM_024453004.1:c.1414C>G
|
XP_024308772.1:p.His472Asp
|
|
XM_024453005.1:c.1396C>G
|
XP_024308773.1:p.His466Asp
|
|
XM_024453006.1:c.1333C>G
|
XP_024308774.1:p.His445Asp
|
|
XR_001739705.1:n.3607-527G>C
|
|
|
XR_923313.2:n.4043-527G>C
|
|
|
NM_000312.4:c.1231C>G
MANE Select
|
NP_000303.1:p.His411Asp
|
|
NM_001375602.1:c.1414C>G
|
NP_001362531.1:p.His472Asp
|
|
NM_001375603.1:c.1396C>G
|
NP_001362532.1:p.His466Asp
|
|
NM_001375604.1:c.1294C>G
|
NP_001362533.1:p.His432Asp
|
|
NM_001375605.1:c.1333C>G
|
NP_001362534.1:p.His445Asp
|
|
NM_001375606.1:c.1399C>G
|
NP_001362535.1:p.His467Asp
|
|
NM_001375607.1:c.1417C>G
|
NP_001362536.1:p.His473Asp
|
|
NM_001375608.1:c.1174C>G
|
NP_001362537.1:p.His392Asp
|
|
NM_001375609.1:c.1207C>G
|
NP_001362538.1:p.His403Asp
|
|
NM_001375610.1:c.1225C>G
|
NP_001362539.1:p.His409Asp
|
|
NM_001375611.1:c.1231C>G
|
NP_001362540.1:p.His411Asp
|
|
NM_001375613.1:c.1231C>G
|
NP_001362542.1:p.His411Asp
|
|