|
ENST00000378043.9:c.614T>C
MANE Select
|
ENSP00000367282.4:p.Ile205Thr
|
|
|
ENST00000378043.8:c.614T>C
|
ENSP00000367282.4:p.Ile205Thr
|
|
|
ENST00000449131.6:c.434T>C
|
ENSP00000399709.2:p.Ile145Thr
|
|
|
ENST00000524877.5:n.1046T>C
|
|
|
|
ENST00000524926.5:c.614T>C
|
ENSP00000432681.1:p.Ile205Thr
|
|
|
ENST00000526988.1:c.296T>C
|
ENSP00000433195.1:p.Ile99Thr
|
|
|
ENST00000529265.5:n.537T>C
|
|
|
|
ENST00000534553.5:c.163+1025T>C
|
ENSP00000431189.1:n.163+1025T>C
|
|
|
NM_001139443.1:c.434T>C
|
NP_001132915.1:p.Ile145Thr
|
|
|
NM_001300786.1:c.434T>C
|
NP_001287715.1:p.Ile145Thr
|
|
|
NM_001300787.1:c.434T>C
|
NP_001287716.1:p.Ile145Thr
|
|
|
NM_004183.3:c.614T>C
|
NP_004174.1:p.Ile205Thr
|
|
|
XM_005274210.2:c.614T>C
|
XP_005274267.1:p.Ile205Thr
|
|
|
XM_005274215.2:c.296T>C
|
XP_005274272.1:p.Ile99Thr
|
|
|
XM_005274216.2:c.434T>C
|
XP_005274273.1:p.Ile145Thr
|
|
|
XM_005274218.3:c.296T>C
|
XP_005274275.1:p.Ile99Thr
|
|
|
XM_005274219.2:c.614T>C
|
XP_005274276.1:p.Ile205Thr
|
|
|
XM_005274221.2:c.614T>C
|
XP_005274278.1:p.Ile205Thr
|
|
|
XM_011545229.1:c.614T>C
|
XP_011543531.1:p.Ile205Thr
|
|
|
XM_011545230.1:c.521T>C
|
XP_011543532.1:p.Ile174Thr
|
|
|
XM_011545231.1:c.296T>C
|
XP_011543533.1:p.Ile99Thr
|
|
|
XM_011545232.1:c.614T>C
|
XP_011543534.1:p.Ile205Thr
|
|
|
NM_001363591.1:c.296T>C
|
NP_001350520.1:p.Ile99Thr
|
|
|
NM_001363592.1:c.614T>C
|
NP_001350521.1:p.Ile205Thr
|
|
|
NM_001363593.1:c.-562T>C
|
NP_001350522.1:n.-562T>C
|
|
|
NR_134580.1:n.1194T>C
|
|
|
|
XM_005274210.4:c.614T>C
|
XP_005274267.1:p.Ile205Thr
|
|
|
XM_005274215.4:c.296T>C
|
XP_005274272.1:p.Ile99Thr
|
|
|
XM_005274216.4:c.434T>C
|
XP_005274273.1:p.Ile145Thr
|
|
|
XM_005274219.4:c.614T>C
|
XP_005274276.1:p.Ile205Thr
|
|
|
XM_005274221.4:c.614T>C
|
XP_005274278.1:p.Ile205Thr
|
|
|
XM_011545229.3:c.614T>C
|
XP_011543531.1:p.Ile205Thr
|
|
|
XM_011545230.3:c.521T>C
|
XP_011543532.1:p.Ile174Thr
|
|
|
XM_017018230.2:c.296T>C
|
XP_016873719.1:p.Ile99Thr
|
|
|
XR_001747952.2:n.1112T>C
|
|
|
|
XR_001747953.2:n.1304T>C
|
|
|
|
XR_001747954.2:n.1304T>C
|
|
|
|
XR_002957249.1:n.762A>G
|
|
|
|
NM_004183.4:c.614T>C
MANE Select
|
NP_004174.1:p.Ile205Thr
|
|
|
NM_001139443.2:c.434T>C
|
NP_001132915.1:p.Ile145Thr
|
|
|
NM_001300786.2:c.434T>C
|
NP_001287715.1:p.Ile145Thr
|
|
|
NM_001300787.2:c.434T>C
|
NP_001287716.1:p.Ile145Thr
|
|
|
NM_001363591.2:c.296T>C
|
NP_001350520.1:p.Ile99Thr
|
|
|
NM_001363593.2:c.-562T>C
|
NP_001350522.1:n.-562T>C
|
|
|
NR_134580.2:n.727T>C
|
|
|
