|
NM_198129.4:c.5596C>T
MANE Select
|
NP_937762.2:p.Gln1866Ter
|
|
ENST00000313654.14:c.5596C>T
MANE Select
|
ENSP00000324532.8:p.Gln1866Ter
|
|
NM_000227.6:c.769C>T
MANE Plus Clinical
|
NP_000218.3:p.Gln257Ter
|
|
ENST00000269217.11:c.769C>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Gln257Ter
|
|
NM_000227.4:c.769C>T
|
NP_000218.3:p.Gln257Ter
|
|
NM_000227.5:c.769C>T
|
NP_000218.3:p.Gln257Ter
|
|
NM_001127717.2:c.5596C>T
|
NP_001121189.2:p.Gln1866Ter
|
|
NM_001127717.3:c.5596C>T
|
NP_001121189.2:p.Gln1866Ter
|
|
NM_001127717.4:c.5596C>T
|
NP_001121189.2:p.Gln1866Ter
|
|
NM_001127718.2:c.769C>T
|
NP_001121190.2:p.Gln257Ter
|
|
NM_001127718.3:c.769C>T
|
NP_001121190.2:p.Gln257Ter
|
|
NM_001127718.4:c.769C>T
|
NP_001121190.2:p.Gln257Ter
|
|
NM_198129.2:c.5596C>T
|
NP_937762.2:p.Gln1866Ter
|
|
NM_198129.3:c.5596C>T
|
NP_937762.2:p.Gln1866Ter
|
|
ENST00000269217.10:c.769C>T
|
ENSP00000269217.5:p.Gln257Ter
|
|
ENST00000313654.13:c.5596C>T
|
ENSP00000324532.8:p.Gln1866Ter
|
|
ENST00000399516.7:c.5596C>T
|
ENSP00000382432.2:p.Gln1866Ter
|
|
ENST00000586751.5:c.374C>T
|
|
|
ENST00000587184.5:c.769C>T
|
ENSP00000466557.1:p.Gln257Ter
|
|
ENST00000649721.1:c.2488C>T
|
ENSP00000497885.1:p.Gln830Ter
|
|
XM_011525978.1:c.5623C>T
|
XP_011524280.1:p.Gln1875Ter
|
|
XM_011525978.2:c.5623C>T
|
XP_011524280.1:p.Gln1875Ter
|
|
XM_011525979.1:c.5614C>T
|
XP_011524281.1:p.Gln1872Ter
|
|
XM_011525979.2:c.5614C>T
|
XP_011524281.1:p.Gln1872Ter
|
|
XM_011525980.1:c.5605C>T
|
XP_011524282.1:p.Gln1869Ter
|
|
XM_011525980.2:c.5605C>T
|
XP_011524282.1:p.Gln1869Ter
|
|
XM_011525981.1:c.5491C>T
|
XP_011524283.1:p.Gln1831Ter
|
|
XM_011525981.2:c.5491C>T
|
XP_011524283.1:p.Gln1831Ter
|
|
XM_011525982.1:c.5623C>T
|
XP_011524284.1:p.Gln1875Ter
|
|
XM_011525982.2:c.5623C>T
|
XP_011524284.1:p.Gln1875Ter
|
|
XM_017025743.1:c.3475C>T
|
XP_016881232.1:p.Gln1159Ter
|
|
XM_017025744.1:c.1165C>T
|
XP_016881233.1:p.Gln389Ter
|
|
XR_001753199.1:n.5864C>T
|
|
