|
ENST00000531904.7:c.7328T>C
|
ENSP00000432391.3:p.Met2443Thr
|
|
|
ENST00000710560.1:c.7319T>C
|
ENSP00000518343.1:p.Met2440Thr
|
|
|
ENST00000649878.2:c.1268T>C
|
ENSP00000497891.2:p.Met423Thr
|
|
|
ENST00000685397.1:c.1268T>C
|
ENSP00000509586.1:p.Met423Thr
|
|
|
ENST00000686370.1:c.1268T>C
|
ENSP00000509179.1:p.Met423Thr
|
|
|
ENST00000689424.1:c.1526T>C
|
ENSP00000509852.1:p.Met509Thr
|
|
|
ENST00000691053.1:c.7301T>C
|
ENSP00000509168.1:p.Met2434Thr
|
|
|
ENST00000389506.10:c.7220T>C
|
ENSP00000374157.5:p.Met2407Thr
|
|
|
ENST00000528278.2:n.6571T>C
|
|
|
|
ENST00000534358.8:c.7229T>C
MANE Select
|
ENSP00000436786.2:p.Met2410Thr
|
|
|
ENST00000649699.1:c.7106T>C
|
ENSP00000496927.1:p.Met2369Thr
|
|
|
ENST00000389506.9:c.7220T>C
|
ENSP00000374157.5:p.Met2407Thr
|
|
|
ENST00000528278.1:n.1356T>C
|
|
|
|
ENST00000534358.5:c.7229T>C
|
ENSP00000436786.1:p.Met2410Thr
|
|
|
NM_001197104.1:c.7229T>C , LRG_613t1:c.7229T>C
|
NP_001184033.1:p.Met2410Thr
|
|
|
NM_005933.3:c.7220T>C
|
NP_005924.2:p.Met2407Thr
|
|
|
XM_006718839.2:c.4712T>C
|
XP_006718902.2:p.Met1571Thr
|
|
|
XM_011542829.1:c.7328T>C
|
XP_011541131.1:p.Met2443Thr
|
|
|
XM_011542830.1:c.7325T>C
|
XP_011541132.1:p.Met2442Thr
|
|
|
XM_011542831.1:c.7319T>C
|
XP_011541133.1:p.Met2440Thr
|
|
|
XM_011542832.1:c.5135T>C
|
XP_011541134.1:p.Met1712Thr
|
|
|
XM_011542833.1:c.4811T>C
|
XP_011541135.1:p.Met1604Thr
|
|
|
XM_006718839.3:c.4712T>C
|
XP_006718902.2:p.Met1571Thr
|
|
|
XM_011542829.2:c.7328T>C
|
XP_011541131.1:p.Met2443Thr
|
|
|
XM_011542830.2:c.7325T>C
|
XP_011541132.1:p.Met2442Thr
|
|
|
XM_011542831.2:c.7319T>C
|
XP_011541133.1:p.Met2440Thr
|
|
|
XM_011542833.2:c.4811T>C
|
XP_011541135.1:p.Met1604Thr
|
|
|
NM_001197104.2:c.7229T>C
MANE Select
|
NP_001184033.1:p.Met2410Thr
|
|
|
NM_005933.4:c.7220T>C
|
NP_005924.2:p.Met2407Thr
|
|
