|
ENST00000641284.2:c.2382-7113G>C
|
ENSP00000493088.1:n.2382-7113G>C
|
|
|
ENST00000646677.2:c.*482G>C
|
ENSP00000496533.1:n.*482G>C
|
|
|
ENST00000697425.1:c.544G>C
|
|
|
|
ENST00000697426.1:c.432G>C
|
|
|
|
ENST00000697427.1:c.348G>C
|
|
|
|
ENST00000697428.1:n.2195G>C
|
|
|
|
ENST00000641284.1:c.2382-7113G>C
|
ENSP00000493088.1:n.2382-7113G>C
|
|
|
ENST00000646677.1:c.*482G>C
|
ENSP00000496533.1:n.*482G>C
|
|
|
ENST00000647318.2:c.2717G>C
MANE Select
|
ENSP00000495993.1:p.Ser906Thr
|
|
|
ENST00000300589.6:c.2798G>C
|
ENSP00000300589.2:p.Ser933Thr
|
|
|
ENST00000524712.5:c.292G>C
|
|
|
|
ENST00000527052.5:c.264G>C
|
|
|
|
ENST00000529633.5:c.376G>C
|
|
|
|
ENST00000534057.1:c.432G>C
|
|
|
|
ENST00000534067.5:c.528G>C
|
|
|
|
NM_001293557.1:c.2717G>C
|
NP_001280486.1:p.Ser906Thr
|
|
|
NM_022162.2:c.2798G>C
|
NP_071445.1:p.Ser933Thr
|
|
|
XM_005256084.2:c.2717G>C
|
XP_005256141.1:p.Ser906Thr
|
|
|
XM_006721242.2:c.2633G>C
|
XP_006721305.1:p.Ser878Thr
|
|
|
XM_011523257.1:c.2294G>C
|
XP_011521559.1:p.Ser765Thr
|
|
|
XM_011523258.1:c.2294G>C
|
XP_011521560.1:p.Ser765Thr
|
|
|
XM_011523259.1:c.2132G>C
|
XP_011521561.1:p.Ser711Thr
|
|
|
XR_429725.2:n.2639G>C
|
|
|
|
XR_429726.2:n.2555G>C
|
|
|
|
XR_933387.1:n.2835G>C
|
|
|
|
XM_005256084.4:c.2717G>C
|
XP_005256141.1:p.Ser906Thr
|
|
|
XM_006721242.4:c.2633G>C
|
XP_006721305.1:p.Ser878Thr
|
|
|
XM_011523259.2:c.2132G>C
|
XP_011521561.1:p.Ser711Thr
|
|
|
XM_017023535.1:c.2225G>C
|
XP_016879024.1:p.Ser742Thr
|
|
|
XM_017023536.1:c.2132G>C
|
XP_016879025.1:p.Ser711Thr
|
|
|
XM_017023537.1:c.2132G>C
|
XP_016879026.1:p.Ser711Thr
|
|
|
XM_017023538.1:c.2132G>C
|
XP_016879027.1:p.Ser711Thr
|
|
|
XR_429725.3:n.2592G>C
|
|
|
|
XR_429726.3:n.2508G>C
|
|
|
|
XR_933387.2:n.2788G>C
|
|
|
|
NM_001293557.2:c.2717G>C
|
NP_001280486.1:p.Ser906Thr
|
|
|
NM_001370466.1:c.2717G>C
MANE Select
|
NP_001357395.1:p.Ser906Thr
|
|
|
NM_022162.3:c.2798G>C
|
NP_071445.1:p.Ser933Thr
|
|
|
NR_163434.1:n.2929G>C
|
|
|
