|
NM_198129.4:c.8851C>T
MANE Select
|
NP_937762.2:p.Arg2951Cys
|
|
ENST00000313654.14:c.8851C>T
MANE Select
|
ENSP00000324532.8:p.Arg2951Cys
|
|
NM_000227.6:c.4024C>T
MANE Plus Clinical
|
NP_000218.3:p.Arg1342Cys
|
|
ENST00000269217.11:c.4024C>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Arg1342Cys
|
|
NM_000227.4:c.4024C>T
|
NP_000218.3:p.Arg1342Cys
|
|
NM_000227.5:c.4024C>T
|
NP_000218.3:p.Arg1342Cys
|
|
NM_001127717.2:c.8683C>T
|
NP_001121189.2:p.Arg2895Cys
|
|
NM_001127717.3:c.8683C>T
|
NP_001121189.2:p.Arg2895Cys
|
|
NM_001127717.4:c.8683C>T
|
NP_001121189.2:p.Arg2895Cys
|
|
NM_001127718.2:c.3856C>T
|
NP_001121190.2:p.Arg1286Cys
|
|
NM_001127718.3:c.3856C>T
|
NP_001121190.2:p.Arg1286Cys
|
|
NM_001127718.4:c.3856C>T
|
NP_001121190.2:p.Arg1286Cys
|
|
NM_198129.2:c.8851C>T
|
NP_937762.2:p.Arg2951Cys
|
|
NM_198129.3:c.8851C>T
|
NP_937762.2:p.Arg2951Cys
|
|
ENST00000269217.10:c.4024C>T
|
ENSP00000269217.5:p.Arg1342Cys
|
|
ENST00000313654.13:c.8851C>T
|
ENSP00000324532.8:p.Arg2951Cys
|
|
ENST00000399516.7:c.8683C>T
|
ENSP00000382432.2:p.Arg2895Cys
|
|
ENST00000587184.5:c.3856C>T
|
ENSP00000466557.1:p.Arg1286Cys
|
|
ENST00000588770.5:n.3429C>T
|
|
|
ENST00000649721.1:c.5446C>T
|
ENSP00000497885.1:p.Arg1816Cys
|
|
XM_011525978.1:c.8878C>T
|
XP_011524280.1:p.Arg2960Cys
|
|
XM_011525978.2:c.8878C>T
|
XP_011524280.1:p.Arg2960Cys
|
|
XM_011525979.1:c.8869C>T
|
XP_011524281.1:p.Arg2957Cys
|
|
XM_011525979.2:c.8869C>T
|
XP_011524281.1:p.Arg2957Cys
|
|
XM_011525980.1:c.8860C>T
|
XP_011524282.1:p.Arg2954Cys
|
|
XM_011525980.2:c.8860C>T
|
XP_011524282.1:p.Arg2954Cys
|
|
XM_011525981.1:c.8746C>T
|
XP_011524283.1:p.Arg2916Cys
|
|
XM_011525981.2:c.8746C>T
|
XP_011524283.1:p.Arg2916Cys
|
|
XM_011525982.1:c.8581C>T
|
XP_011524284.1:p.Arg2861Cys
|
|
XM_011525982.2:c.8581C>T
|
XP_011524284.1:p.Arg2861Cys
|
|
XM_017025743.1:c.6730C>T
|
XP_016881232.1:p.Arg2244Cys
|
|
XM_017025744.1:c.4420C>T
|
XP_016881233.1:p.Arg1474Cys
|
|
XR_001753199.1:n.9119C>T
|
|
