|
ENST00000361492.9:c.4616T>C
MANE Select
|
ENSP00000354586.5:p.Ile1539Thr
|
|
|
ENST00000452319.6:c.4667T>C
|
ENSP00000390436.1:p.Ile1556Thr
|
|
|
ENST00000341310.10:c.*3715T>C
|
ENSP00000344473.6:n.*3715T>C
|
|
|
ENST00000361492.8:c.4667T>C
|
ENSP00000354586.4:p.Ile1556Thr
|
|
|
ENST00000438299.5:c.*2544-9T>C
|
ENSP00000400593.1:n.*2544-9T>C
|
|
|
ENST00000445186.5:c.*3766T>C
|
ENSP00000397488.1:n.*3766T>C
|
|
|
ENST00000452319.5:c.4667T>C
|
ENSP00000390436.1:p.Ile1556Thr
|
|
|
ENST00000452692.5:c.*2493-9T>C
|
ENSP00000403715.1:n.*2493-9T>C
|
|
|
NM_005270.4:c.4667T>C
|
NP_005261.2:p.Ile1556Thr
|
|
|
XM_006712422.1:c.4616T>C
|
XP_006712485.1:p.Ile1539Thr
|
|
|
XM_011510969.1:c.4649T>C
|
XP_011509271.1:p.Ile1550Thr
|
|
|
XM_011510970.1:c.4526T>C
|
XP_011509272.1:p.Ile1509Thr
|
|
|
XM_011510971.1:c.4472T>C
|
XP_011509273.1:p.Ile1491Thr
|
|
|
XM_011510972.1:c.4472T>C
|
XP_011509274.1:p.Ile1491Thr
|
|
|
XM_011510973.1:c.4292T>C
|
XP_011509275.1:p.Ile1431Thr
|
|
|
XM_011510974.1:c.4241T>C
|
XP_011509276.1:p.Ile1414Thr
|
|
|
XM_006712422.3:c.4616T>C
|
XP_006712485.1:p.Ile1539Thr
|
|
|
XM_011510969.2:c.4919T>C
|
XP_011509271.2:p.Ile1640Thr
|
|
|
XM_011510970.2:c.4526T>C
|
XP_011509272.1:p.Ile1509Thr
|
|
|
XM_011510971.2:c.4472T>C
|
XP_011509273.1:p.Ile1491Thr
|
|
|
XM_011510972.2:c.4568T>C
|
XP_011509274.2:p.Ile1523Thr
|
|
|
XM_011510973.2:c.4292T>C
|
XP_011509275.1:p.Ile1431Thr
|
|
|
XM_011510974.2:c.4241T>C
|
XP_011509276.1:p.Ile1414Thr
|
|
|
XM_017003818.1:c.4868T>C
|
XP_016859307.1:p.Ile1623Thr
|
|
|
XM_024452794.1:c.4667T>C
|
XP_024308562.1:p.Ile1556Thr
|
|
|
XM_024452795.1:c.4667T>C
|
XP_024308563.1:p.Ile1556Thr
|
|
|
NM_001371271.1:c.4667T>C
|
NP_001358200.1:p.Ile1556Thr
|
|
|
NM_001374353.1:c.4616T>C
MANE Select
|
NP_001361282.1:p.Ile1539Thr
|
|
|
NM_001374354.1:c.4241T>C
|
NP_001361283.1:p.Ile1414Thr
|
|
|
NM_005270.5:c.4667T>C
|
NP_005261.2:p.Ile1556Thr
|
|
