|
ENST00000234071.8:c.1152dup
MANE Select
|
ENSP00000234071.4:p.Met385HisfsTer?
|
|
|
ENST00000234071.7:c.1152dup
|
ENSP00000234071.3:p.Met385HisfsTer?
|
|
|
ENST00000402125.2:c.476dup
|
|
|
|
ENST00000409048.1:c.1254dup
|
ENSP00000386679.1:p.Met419HisfsTer?
|
|
|
NM_000312.3:c.1152dup , LRG_599t1:c.1152dup
|
NP_000303.1:p.Met385HisfsTer?
|
|
|
XM_005263715.3:c.1335dup
|
XP_005263772.1:p.Met446HisfsTer?
|
|
|
XM_005263716.3:c.1317dup
|
XP_005263773.1:p.Met440HisfsTer?
|
|
|
XM_005263717.3:c.1215dup
|
XP_005263774.1:p.Met406HisfsTer?
|
|
|
XR_923313.1:n.1332-448dup
|
|
|
|
XM_005263717.4:c.1215dup
|
XP_005263774.1:p.Met406HisfsTer?
|
|
|
XM_017004505.1:c.1395dup
|
XP_016859994.1:p.Met466HisfsTer?
|
|
|
XM_024453002.1:c.1497dup
|
XP_024308770.1:p.Met500HisfsTer?
|
|
|
XM_024453003.1:c.1437dup
|
XP_024308771.1:p.Met480HisfsTer?
|
|
|
XM_024453004.1:c.1335dup
|
XP_024308772.1:p.Met446HisfsTer?
|
|
|
XM_024453005.1:c.1317dup
|
XP_024308773.1:p.Met440HisfsTer?
|
|
|
XM_024453006.1:c.1254dup
|
XP_024308774.1:p.Met419HisfsTer?
|
|
|
XR_001739705.1:n.3607-448dup
|
|
|
|
XR_923313.2:n.4043-448dup
|
|
|
|
NM_000312.4:c.1152dup
MANE Select
|
NP_000303.1:p.Met385HisfsTer?
|
|
|
NM_001375602.1:c.1335dup
|
NP_001362531.1:p.Met446HisfsTer?
|
|
|
NM_001375603.1:c.1317dup
|
NP_001362532.1:p.Met440HisfsTer?
|
|
|
NM_001375604.1:c.1215dup
|
NP_001362533.1:p.Met406HisfsTer?
|
|
|
NM_001375605.1:c.1254dup
|
NP_001362534.1:p.Met419HisfsTer?
|
|
|
NM_001375606.1:c.1320dup
|
NP_001362535.1:p.Met441HisfsTer?
|
|
|
NM_001375607.1:c.1338dup
|
NP_001362536.1:p.Met447HisfsTer?
|
|
|
NM_001375608.1:c.1095dup
|
NP_001362537.1:p.Met366HisfsTer?
|
|
|
NM_001375609.1:c.1128dup
|
NP_001362538.1:p.Met377HisfsTer?
|
|
|
NM_001375610.1:c.1146dup
|
NP_001362539.1:p.Met383HisfsTer?
|
|
|
NM_001375611.1:c.1152dup
|
NP_001362540.1:p.Met385HisfsTer?
|
|
|
NM_001375613.1:c.1152dup
|
NP_001362542.1:p.Met385HisfsTer?
|
|
