ENST00000234071.8:c.635T>G
MANE Select
|
ENSP00000234071.4:p.Leu212Arg
|
|
ENST00000234071.7:c.635T>G
|
ENSP00000234071.3:p.Leu212Arg
|
|
ENST00000402125.2:c.121-2173T>G
|
|
|
ENST00000409048.1:c.737T>G
|
ENSP00000386679.1:p.Leu246Arg
|
|
ENST00000464089.1:n.221T>G
|
|
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NM_000312.3:c.635T>G , LRG_599t1:c.635T>G
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NP_000303.1:p.Leu212Arg
|
|
XM_005263715.3:c.818T>G
|
XP_005263772.1:p.Leu273Arg
|
|
XM_005263716.3:c.800T>G
|
XP_005263773.1:p.Leu267Arg
|
|
XM_005263717.3:c.698T>G
|
XP_005263774.1:p.Leu233Arg
|
|
XM_005263717.4:c.698T>G
|
XP_005263774.1:p.Leu233Arg
|
|
XM_017004505.1:c.878T>G
|
XP_016859994.1:p.Leu293Arg
|
|
XM_024453002.1:c.980T>G
|
XP_024308770.1:p.Leu327Arg
|
|
XM_024453003.1:c.920T>G
|
XP_024308771.1:p.Leu307Arg
|
|
XM_024453004.1:c.818T>G
|
XP_024308772.1:p.Leu273Arg
|
|
XM_024453005.1:c.800T>G
|
XP_024308773.1:p.Leu267Arg
|
|
XM_024453006.1:c.737T>G
|
XP_024308774.1:p.Leu246Arg
|
|
XR_923313.2:n.4401A>C
|
|
|
NM_000312.4:c.635T>G
MANE Select
|
NP_000303.1:p.Leu212Arg
|
|
NM_001375602.1:c.818T>G
|
NP_001362531.1:p.Leu273Arg
|
|
NM_001375603.1:c.800T>G
|
NP_001362532.1:p.Leu267Arg
|
|
NM_001375604.1:c.698T>G
|
NP_001362533.1:p.Leu233Arg
|
|
NM_001375605.1:c.737T>G
|
NP_001362534.1:p.Leu246Arg
|
|
NM_001375606.1:c.803T>G
|
NP_001362535.1:p.Leu268Arg
|
|
NM_001375607.1:c.821T>G
|
NP_001362536.1:p.Leu274Arg
|
|
NM_001375608.1:c.578T>G
|
NP_001362537.1:p.Leu193Arg
|
|
NM_001375609.1:c.611T>G
|
NP_001362538.1:p.Leu204Arg
|
|
NM_001375610.1:c.629T>G
|
NP_001362539.1:p.Leu210Arg
|
|
NM_001375611.1:c.635T>G
|
NP_001362540.1:p.Leu212Arg
|
|
NM_001375613.1:c.635T>G
|
NP_001362542.1:p.Leu212Arg
|
|