ENST00000234071.8:c.673T>C
MANE Select
|
ENSP00000234071.4:p.Trp225Arg
|
|
ENST00000234071.7:c.673T>C
|
ENSP00000234071.3:p.Trp225Arg
|
|
ENST00000402125.2:c.121-2135T>C
|
|
|
ENST00000409048.1:c.775T>C
|
ENSP00000386679.1:p.Trp259Arg
|
|
ENST00000464089.1:n.259T>C
|
|
|
NM_000312.3:c.673T>C , LRG_599t1:c.673T>C
|
NP_000303.1:p.Trp225Arg
|
|
XM_005263715.3:c.856T>C
|
XP_005263772.1:p.Trp286Arg
|
|
XM_005263716.3:c.838T>C
|
XP_005263773.1:p.Trp280Arg
|
|
XM_005263717.3:c.736T>C
|
XP_005263774.1:p.Trp246Arg
|
|
XM_005263717.4:c.736T>C
|
XP_005263774.1:p.Trp246Arg
|
|
XM_017004505.1:c.916T>C
|
XP_016859994.1:p.Trp306Arg
|
|
XM_024453002.1:c.1018T>C
|
XP_024308770.1:p.Trp340Arg
|
|
XM_024453003.1:c.958T>C
|
XP_024308771.1:p.Trp320Arg
|
|
XM_024453004.1:c.856T>C
|
XP_024308772.1:p.Trp286Arg
|
|
XM_024453005.1:c.838T>C
|
XP_024308773.1:p.Trp280Arg
|
|
XM_024453006.1:c.775T>C
|
XP_024308774.1:p.Trp259Arg
|
|
XR_923313.2:n.4363A>G
|
|
|
NM_000312.4:c.673T>C
MANE Select
|
NP_000303.1:p.Trp225Arg
|
|
NM_001375602.1:c.856T>C
|
NP_001362531.1:p.Trp286Arg
|
|
NM_001375603.1:c.838T>C
|
NP_001362532.1:p.Trp280Arg
|
|
NM_001375604.1:c.736T>C
|
NP_001362533.1:p.Trp246Arg
|
|
NM_001375605.1:c.775T>C
|
NP_001362534.1:p.Trp259Arg
|
|
NM_001375606.1:c.841T>C
|
NP_001362535.1:p.Trp281Arg
|
|
NM_001375607.1:c.859T>C
|
NP_001362536.1:p.Trp287Arg
|
|
NM_001375608.1:c.616T>C
|
NP_001362537.1:p.Trp206Arg
|
|
NM_001375609.1:c.649T>C
|
NP_001362538.1:p.Trp217Arg
|
|
NM_001375610.1:c.667T>C
|
NP_001362539.1:p.Trp223Arg
|
|
NM_001375611.1:c.673T>C
|
NP_001362540.1:p.Trp225Arg
|
|
NM_001375613.1:c.673T>C
|
NP_001362542.1:p.Trp225Arg
|
|