|
NM_198129.4:c.8941C>T
MANE Select
|
NP_937762.2:p.Gln2981Ter
|
|
ENST00000313654.14:c.8941C>T
MANE Select
|
ENSP00000324532.8:p.Gln2981Ter
|
|
NM_000227.6:c.4114C>T
MANE Plus Clinical
|
NP_000218.3:p.Gln1372Ter
|
|
ENST00000269217.11:c.4114C>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Gln1372Ter
|
|
NM_000227.4:c.4114C>T
|
NP_000218.3:p.Gln1372Ter
|
|
NM_000227.5:c.4114C>T
|
NP_000218.3:p.Gln1372Ter
|
|
NM_001127717.2:c.8773C>T
|
NP_001121189.2:p.Gln2925Ter
|
|
NM_001127717.3:c.8773C>T
|
NP_001121189.2:p.Gln2925Ter
|
|
NM_001127717.4:c.8773C>T
|
NP_001121189.2:p.Gln2925Ter
|
|
NM_001127718.2:c.3946C>T
|
NP_001121190.2:p.Gln1316Ter
|
|
NM_001127718.3:c.3946C>T
|
NP_001121190.2:p.Gln1316Ter
|
|
NM_001127718.4:c.3946C>T
|
NP_001121190.2:p.Gln1316Ter
|
|
NM_198129.2:c.8941C>T
|
NP_937762.2:p.Gln2981Ter
|
|
NM_198129.3:c.8941C>T
|
NP_937762.2:p.Gln2981Ter
|
|
ENST00000269217.10:c.4114C>T
|
ENSP00000269217.5:p.Gln1372Ter
|
|
ENST00000313654.13:c.8941C>T
|
ENSP00000324532.8:p.Gln2981Ter
|
|
ENST00000399516.7:c.8773C>T
|
ENSP00000382432.2:p.Gln2925Ter
|
|
ENST00000587184.5:c.3946C>T
|
ENSP00000466557.1:p.Gln1316Ter
|
|
ENST00000588770.5:n.3519C>T
|
|
|
ENST00000649721.1:c.5536C>T
|
ENSP00000497885.1:p.Gln1846Ter
|
|
XM_011525978.1:c.8968C>T
|
XP_011524280.1:p.Gln2990Ter
|
|
XM_011525978.2:c.8968C>T
|
XP_011524280.1:p.Gln2990Ter
|
|
XM_011525979.1:c.8959C>T
|
XP_011524281.1:p.Gln2987Ter
|
|
XM_011525979.2:c.8959C>T
|
XP_011524281.1:p.Gln2987Ter
|
|
XM_011525980.1:c.8950C>T
|
XP_011524282.1:p.Gln2984Ter
|
|
XM_011525980.2:c.8950C>T
|
XP_011524282.1:p.Gln2984Ter
|
|
XM_011525981.1:c.8836C>T
|
XP_011524283.1:p.Gln2946Ter
|
|
XM_011525981.2:c.8836C>T
|
XP_011524283.1:p.Gln2946Ter
|
|
XM_011525982.1:c.8671C>T
|
XP_011524284.1:p.Gln2891Ter
|
|
XM_011525982.2:c.8671C>T
|
XP_011524284.1:p.Gln2891Ter
|
|
XM_017025743.1:c.6820C>T
|
XP_016881232.1:p.Gln2274Ter
|
|
XM_017025744.1:c.4510C>T
|
XP_016881233.1:p.Gln1504Ter
|
|
XR_001753199.1:n.9209C>T
|
|
