|
ENST00000641284.2:c.2382-7121G>T
|
ENSP00000493088.1:n.2382-7121G>T
|
|
|
ENST00000646677.2:c.*474G>T
|
ENSP00000496533.1:n.*474G>T
|
|
|
ENST00000697425.1:c.536G>T
|
|
|
|
ENST00000697426.1:c.424G>T
|
|
|
|
ENST00000697427.1:c.340G>T
|
|
|
|
ENST00000697428.1:n.2187G>T
|
|
|
|
ENST00000641284.1:c.2382-7121G>T
|
ENSP00000493088.1:n.2382-7121G>T
|
|
|
ENST00000646677.1:c.*474G>T
|
ENSP00000496533.1:n.*474G>T
|
|
|
ENST00000647318.2:c.2709G>T
MANE Select
|
ENSP00000495993.1:p.Arg903Ser
|
|
|
ENST00000300589.6:c.2790G>T
|
ENSP00000300589.2:p.Arg930Ser
|
|
|
ENST00000524712.5:c.284G>T
|
|
|
|
ENST00000527052.5:c.256G>T
|
|
|
|
ENST00000529633.5:c.368G>T
|
|
|
|
ENST00000534057.1:c.424G>T
|
|
|
|
ENST00000534067.5:c.520G>T
|
|
|
|
NM_001293557.1:c.2709G>T
|
NP_001280486.1:p.Arg903Ser
|
|
|
NM_022162.2:c.2790G>T
|
NP_071445.1:p.Arg930Ser
|
|
|
XM_005256084.2:c.2709G>T
|
XP_005256141.1:p.Arg903Ser
|
|
|
XM_006721242.2:c.2625G>T
|
XP_006721305.1:p.Arg875Ser
|
|
|
XM_011523257.1:c.2286G>T
|
XP_011521559.1:p.Arg762Ser
|
|
|
XM_011523258.1:c.2286G>T
|
XP_011521560.1:p.Arg762Ser
|
|
|
XM_011523259.1:c.2124G>T
|
XP_011521561.1:p.Arg708Ser
|
|
|
XR_429725.2:n.2631G>T
|
|
|
|
XR_429726.2:n.2547G>T
|
|
|
|
XR_933387.1:n.2827G>T
|
|
|
|
XM_005256084.4:c.2709G>T
|
XP_005256141.1:p.Arg903Ser
|
|
|
XM_006721242.4:c.2625G>T
|
XP_006721305.1:p.Arg875Ser
|
|
|
XM_011523259.2:c.2124G>T
|
XP_011521561.1:p.Arg708Ser
|
|
|
XM_017023535.1:c.2217G>T
|
XP_016879024.1:p.Arg739Ser
|
|
|
XM_017023536.1:c.2124G>T
|
XP_016879025.1:p.Arg708Ser
|
|
|
XM_017023537.1:c.2124G>T
|
XP_016879026.1:p.Arg708Ser
|
|
|
XM_017023538.1:c.2124G>T
|
XP_016879027.1:p.Arg708Ser
|
|
|
XR_429725.3:n.2584G>T
|
|
|
|
XR_429726.3:n.2500G>T
|
|
|
|
XR_933387.2:n.2780G>T
|
|
|
|
NM_001293557.2:c.2709G>T
|
NP_001280486.1:p.Arg903Ser
|
|
|
NM_001370466.1:c.2709G>T
MANE Select
|
NP_001357395.1:p.Arg903Ser
|
|
|
NM_022162.3:c.2790G>T
|
NP_071445.1:p.Arg930Ser
|
|
|
NR_163434.1:n.2921G>T
|
|
|
