ENST00000373344.11:c.7442G>C
MANE Select
|
ENSP00000362441.4:p.Ser2481Thr
|
|
ENST00000675732.1:c.2540G>C
|
ENSP00000502598.1:p.Ser847Thr
|
|
ENST00000373344.9:c.7442G>C
|
ENSP00000362441.4:p.Ser2481Thr
|
|
ENST00000395603.7:c.7328G>C
|
ENSP00000378967.3:p.Ser2443Thr
|
|
ENST00000480283.5:c.*7070G>C
|
ENSP00000480196.1:n.*7070G>C
|
|
ENST00000623706.3:n.5762G>C
|
|
|
NM_000489.4:c.7442G>C
|
NP_000480.3:p.Ser2481Thr
|
|
NM_138270.3:c.7328G>C
|
NP_612114.2:p.Ser2443Thr
|
|
XM_005262153.3:c.7439G>C
|
XP_005262210.2:p.Ser2480Thr
|
|
XM_005262154.3:c.7355G>C
|
XP_005262211.2:p.Ser2452Thr
|
|
XM_005262155.3:c.7325G>C
|
XP_005262212.2:p.Ser2442Thr
|
|
XM_005262156.3:c.7277G>C
|
XP_005262213.2:p.Ser2426Thr
|
|
XM_005262157.3:c.7238G>C
|
XP_005262214.2:p.Ser2413Thr
|
|
XM_006724666.2:c.7325G>C
|
XP_006724729.1:p.Ser2442Thr
|
|
XM_006724667.2:c.7163G>C
|
XP_006724730.1:p.Ser2388Thr
|
|
XR_938400.1:n.9034G>C
|
|
|
NM_000489.5:c.7442G>C
|
NP_000480.3:p.Ser2481Thr
|
|
XM_005262153.5:c.7439G>C
|
XP_005262210.2:p.Ser2480Thr
|
|
XM_005262154.5:c.7355G>C
|
XP_005262211.2:p.Ser2452Thr
|
|
XM_005262155.4:c.7325G>C
|
XP_005262212.2:p.Ser2442Thr
|
|
XM_005262156.4:c.7277G>C
|
XP_005262213.2:p.Ser2426Thr
|
|
XM_005262157.5:c.7238G>C
|
XP_005262214.2:p.Ser2413Thr
|
|
XM_006724666.4:c.7325G>C
|
XP_006724729.1:p.Ser2442Thr
|
|
XM_006724667.3:c.7163G>C
|
XP_006724730.1:p.Ser2388Thr
|
|
XM_017029601.2:c.7352G>C
|
XP_016885090.1:p.Ser2451Thr
|
|
XM_017029602.1:c.7322G>C
|
XP_016885091.1:p.Ser2441Thr
|
|
XM_017029603.1:c.7274G>C
|
XP_016885092.1:p.Ser2425Thr
|
|
XM_017029604.2:c.7241G>C
|
XP_016885093.1:p.Ser2414Thr
|
|
XM_017029605.1:c.7238G>C
|
XP_016885094.1:p.Ser2413Thr
|
|
XM_017029606.2:c.7211G>C
|
XP_016885095.1:p.Ser2404Thr
|
|
XM_017029607.2:c.7208G>C
|
XP_016885096.1:p.Ser2403Thr
|
|
XM_017029608.2:c.7160G>C
|
XP_016885097.1:p.Ser2387Thr
|
|
XM_017029609.1:c.7124G>C
|
XP_016885098.1:p.Ser2375Thr
|
|
XM_017029610.1:c.7121G>C
|
XP_016885099.1:p.Ser2374Thr
|
|
XM_017029611.1:c.7076G>C
|
XP_016885100.1:p.Ser2359Thr
|
|
XR_001755700.2:n.7741G>C
|
|
|
NM_138270.4:c.7328G>C
|
NP_612114.2:p.Ser2443Thr
|
|
NM_000489.6:c.7442G>C
MANE Select
|
NP_000480.3:p.Ser2481Thr
|
|
NM_138270.5:c.7328G>C
|
NP_612114.2:p.Ser2443Thr
|
|