ENST00000334636.10:c.1313T>C
MANE Select
|
ENSP00000334592.5:p.Leu438Ser
|
|
ENST00000334636.9:c.1313T>C
|
ENSP00000334592.5:p.Leu438Ser
|
|
ENST00000525015.1:c.143T>C
|
|
|
ENST00000530609.5:c.*909T>C
|
ENSP00000466060.1:n.*909T>C
|
|
ENST00000532378.5:c.614T>C
|
ENSP00000435484.1:p.Leu205Ser
|
|
ENST00000532805.1:c.*421T>C
|
ENSP00000465097.1:n.*421T>C
|
|
ENST00000534686.5:c.*673T>C
|
ENSP00000432087.2:n.*673T>C
|
|
NM_024514.4:c.1313T>C
|
NP_078790.2:p.Leu438Ser
|
|
XM_005252788.1:c.1169T>C
|
XP_005252845.1:p.Leu390Ser
|
|
XM_005252789.2:c.1151T>C
|
XP_005252846.1:p.Leu384Ser
|
|
XM_005252791.3:c.968T>C
|
XP_005252848.1:p.Leu323Ser
|
|
XM_006718142.2:c.1268T>C
|
XP_006718205.1:p.Leu423Ser
|
|
XM_011519894.1:c.968T>C
|
XP_011518196.1:p.Leu323Ser
|
|
XM_011519895.1:c.968T>C
|
XP_011518197.1:p.Leu323Ser
|
|
XM_011519896.1:c.968T>C
|
XP_011518198.1:p.Leu323Ser
|
|
XM_011519897.1:c.968T>C
|
XP_011518199.1:p.Leu323Ser
|
|
XM_011519898.1:c.968T>C
|
XP_011518200.1:p.Leu323Ser
|
|
XR_242777.2:n.1130T>C
|
|
|
XM_005252788.2:c.1169T>C
|
XP_005252845.1:p.Leu390Ser
|
|
XM_005252789.3:c.1151T>C
|
XP_005252846.1:p.Leu384Ser
|
|
XM_011519895.2:c.968T>C
|
XP_011518197.1:p.Leu323Ser
|
|
XM_011519898.3:c.968T>C
|
XP_011518200.1:p.Leu323Ser
|
|
XM_017017190.2:c.1148T>C
|
XP_016872679.1:p.Leu383Ser
|
|
XM_017017191.2:c.968T>C
|
XP_016872680.1:p.Leu323Ser
|
|
XM_017017192.2:c.968T>C
|
XP_016872681.1:p.Leu323Ser
|
|
XM_017017193.2:c.968T>C
|
XP_016872682.1:p.Leu323Ser
|
|
XM_017017194.2:c.968T>C
|
XP_016872683.1:p.Leu323Ser
|
|
XM_024448345.1:c.1148T>C
|
XP_024304113.1:p.Leu383Ser
|
|
XM_024448346.1:c.968T>C
|
XP_024304114.1:p.Leu323Ser
|
|
XM_024448347.1:c.968T>C
|
XP_024304115.1:p.Leu323Ser
|
|
XM_024448348.1:c.968T>C
|
XP_024304116.1:p.Leu323Ser
|
|
XR_002957123.1:n.1093T>C
|
|
|
XR_002957124.1:n.1359T>C
|
|
|
XR_242777.3:n.1130T>C
|
|
|
NM_001377214.1:c.968T>C
|
NP_001364143.1:p.Leu323Ser
|
|
NM_001377215.1:c.968T>C
|
NP_001364144.1:p.Leu323Ser
|
|
NM_001377216.1:c.968T>C
|
NP_001364145.1:p.Leu323Ser
|
|
NM_001377217.1:c.1151T>C
|
NP_001364146.1:p.Leu384Ser
|
|
NM_001377227.1:c.968T>C
|
NP_001364156.1:p.Leu323Ser
|
|
NM_024514.5:c.1313T>C
MANE Select
|
NP_078790.2:p.Leu438Ser
|
|
NM_001400558.1:c.968T>C
|
NP_001387487.1:p.Leu323Ser
|
|
NM_001400559.1:c.968T>C
|
NP_001387488.1:p.Leu323Ser
|
|
NM_001400560.1:c.968T>C
|
NP_001387489.1:p.Leu323Ser
|
|
NM_001400561.1:c.968T>C
|
NP_001387490.1:p.Leu323Ser
|
|
NM_001400562.1:c.614T>C
|
NP_001387491.1:p.Leu205Ser
|
|
NM_001400563.1:c.614T>C
|
NP_001387492.1:p.Leu205Ser
|
|
NM_001400564.1:c.614T>C
|
NP_001387493.1:p.Leu205Ser
|
|
NM_001400565.1:c.614T>C
|
NP_001387494.1:p.Leu205Ser
|
|
NM_001400566.1:c.335T>C
|
NP_001387495.1:p.Leu112Ser
|
|
NM_001400567.1:c.1169T>C
|
NP_001387496.1:p.Leu390Ser
|
|
NM_001400568.1:c.1268T>C
|
NP_001387497.1:p.Leu423Ser
|
|
NR_174512.1:n.1180T>C
|
|
|
NR_174513.1:n.1029T>C
|
|
|
NR_174514.1:n.1404T>C
|
|
|
NR_174515.1:n.1813T>C
|
|
|
NR_174516.1:n.991T>C
|
|
|
NR_174517.1:n.527T>C
|
|
|
NR_174518.1:n.1624T>C
|
|
|
NR_174519.1:n.1371T>C
|
|
|
NR_174520.1:n.1162T>C
|
|
|
NR_174521.1:n.1662T>C
|
|
|
NR_174522.1:n.1160T>C
|
|
|
NR_174523.1:n.1571T>C
|
|
|