ENST00000234071.8:c.1205G>C
MANE Select
|
ENSP00000234071.4:p.Ser402Thr
|
|
ENST00000234071.7:c.1205G>C
|
ENSP00000234071.3:p.Ser402Thr
|
|
ENST00000402125.2:c.529G>C
|
|
|
ENST00000409048.1:c.1307G>C
|
ENSP00000386679.1:p.Ser436Thr
|
|
NM_000312.3:c.1205G>C , LRG_599t1:c.1205G>C
|
NP_000303.1:p.Ser402Thr
|
|
XM_005263715.3:c.1388G>C
|
XP_005263772.1:p.Ser463Thr
|
|
XM_005263716.3:c.1370G>C
|
XP_005263773.1:p.Ser457Thr
|
|
XM_005263717.3:c.1268G>C
|
XP_005263774.1:p.Ser423Thr
|
|
XR_923313.1:n.1332-501C>G
|
|
|
XM_005263717.4:c.1268G>C
|
XP_005263774.1:p.Ser423Thr
|
|
XM_017004505.1:c.1448G>C
|
XP_016859994.1:p.Ser483Thr
|
|
XM_024453002.1:c.1550G>C
|
XP_024308770.1:p.Ser517Thr
|
|
XM_024453003.1:c.1490G>C
|
XP_024308771.1:p.Ser497Thr
|
|
XM_024453004.1:c.1388G>C
|
XP_024308772.1:p.Ser463Thr
|
|
XM_024453005.1:c.1370G>C
|
XP_024308773.1:p.Ser457Thr
|
|
XM_024453006.1:c.1307G>C
|
XP_024308774.1:p.Ser436Thr
|
|
XR_001739705.1:n.3607-501C>G
|
|
|
XR_923313.2:n.4043-501C>G
|
|
|
NM_000312.4:c.1205G>C
MANE Select
|
NP_000303.1:p.Ser402Thr
|
|
NM_001375602.1:c.1388G>C
|
NP_001362531.1:p.Ser463Thr
|
|
NM_001375603.1:c.1370G>C
|
NP_001362532.1:p.Ser457Thr
|
|
NM_001375604.1:c.1268G>C
|
NP_001362533.1:p.Ser423Thr
|
|
NM_001375605.1:c.1307G>C
|
NP_001362534.1:p.Ser436Thr
|
|
NM_001375606.1:c.1373G>C
|
NP_001362535.1:p.Ser458Thr
|
|
NM_001375607.1:c.1391G>C
|
NP_001362536.1:p.Ser464Thr
|
|
NM_001375608.1:c.1148G>C
|
NP_001362537.1:p.Ser383Thr
|
|
NM_001375609.1:c.1181G>C
|
NP_001362538.1:p.Ser394Thr
|
|
NM_001375610.1:c.1199G>C
|
NP_001362539.1:p.Ser400Thr
|
|
NM_001375611.1:c.1205G>C
|
NP_001362540.1:p.Ser402Thr
|
|
NM_001375613.1:c.1205G>C
|
NP_001362542.1:p.Ser402Thr
|
|