|
ENST00000234071.8:c.797-60A>G
MANE Select
|
ENSP00000234071.4:n.797-60A>G
|
|
|
ENST00000234071.7:c.797-60A>G
|
ENSP00000234071.3:n.797-60A>G
|
|
|
ENST00000402125.2:c.121-60A>G
|
|
|
|
ENST00000409048.1:c.899-60A>G
|
ENSP00000386679.1:n.899-60A>G
|
|
|
NM_000312.3:c.797-60A>G , LRG_599t1:c.797-60A>G
|
NP_000303.1:n.797-60A>G
|
|
|
XM_005263715.3:c.980-60A>G
|
XP_005263772.1:n.980-60A>G
|
|
|
XM_005263716.3:c.962-60A>G
|
XP_005263773.1:n.962-60A>G
|
|
|
XM_005263717.3:c.860-60A>G
|
XP_005263774.1:n.860-60A>G
|
|
|
XR_923313.1:n.1332-33T>C
|
|
|
|
XM_005263717.4:c.860-60A>G
|
XP_005263774.1:n.860-60A>G
|
|
|
XM_017004505.1:c.1040-60A>G
|
XP_016859994.1:n.1040-60A>G
|
|
|
XM_024453002.1:c.1142-60A>G
|
XP_024308770.1:n.1142-60A>G
|
|
|
XM_024453003.1:c.1082-60A>G
|
XP_024308771.1:n.1082-60A>G
|
|
|
XM_024453004.1:c.980-60A>G
|
XP_024308772.1:n.980-60A>G
|
|
|
XM_024453005.1:c.962-60A>G
|
XP_024308773.1:n.962-60A>G
|
|
|
XM_024453006.1:c.899-60A>G
|
XP_024308774.1:n.899-60A>G
|
|
|
XR_001739705.1:n.3607-33T>C
|
|
|
|
XR_923313.2:n.4043-33T>C
|
|
|
|
NM_000312.4:c.797-60A>G
MANE Select
|
NP_000303.1:n.797-60A>G
|
|
|
NM_001375602.1:c.980-60A>G
|
NP_001362531.1:n.980-60A>G
|
|
|
NM_001375603.1:c.962-60A>G
|
NP_001362532.1:n.962-60A>G
|
|
|
NM_001375604.1:c.860-60A>G
|
NP_001362533.1:n.860-60A>G
|
|
|
NM_001375605.1:c.899-60A>G
|
NP_001362534.1:n.899-60A>G
|
|
|
NM_001375606.1:c.965-60A>G
|
NP_001362535.1:n.965-60A>G
|
|
|
NM_001375607.1:c.983-60A>G
|
NP_001362536.1:n.983-60A>G
|
|
|
NM_001375608.1:c.740-60A>G
|
NP_001362537.1:n.740-60A>G
|
|
|
NM_001375609.1:c.773-60A>G
|
NP_001362538.1:n.773-60A>G
|
|
|
NM_001375610.1:c.791-60A>G
|
NP_001362539.1:n.791-60A>G
|
|
|
NM_001375611.1:c.797-60A>G
|
NP_001362540.1:n.797-60A>G
|
|
|
NM_001375613.1:c.797-60A>G
|
NP_001362542.1:n.797-60A>G
|
|
