ENST00000356487.11:c.1478T>G
MANE Select
|
ENSP00000348877.3:p.Met493Arg
|
|
ENST00000415930.8:c.1595T>G
|
ENSP00000405573.3:p.Met532Arg
|
|
ENST00000586425.2:c.1158-14T>G
|
|
|
ENST00000588991.7:c.1511T>G
|
ENSP00000465858.3:p.Met504Arg
|
|
ENST00000643067.1:n.2523T>G
|
|
|
ENST00000647446.1:c.*529T>G
|
ENSP00000495129.1:n.*529T>G
|
|
ENST00000356487.9:c.1478T>G
|
ENSP00000348877.3:p.Met493Arg
|
|
ENST00000415930.7:c.1511T>G
|
ENSP00000405573.2:p.Met504Arg
|
|
ENST00000586077.1:n.2440T>G
|
|
|
ENST00000586392.1:n.1216T>G
|
|
|
ENST00000586425.1:c.1399-179T>G
|
ENSP00000467670.2:n.1399-179T>G
|
|
ENST00000588991.6:c.1523T>G
|
ENSP00000465858.2:p.Met508Arg
|
|
ENST00000592740.5:c.193+3065T>G
|
|
|
NM_000175.3:c.1478T>G
|
NP_000166.2:p.Met493Arg
|
|
NM_001184722.1:c.1511T>G
|
NP_001171651.1:p.Met504Arg
|
|
NM_001289789.1:c.1595T>G
|
NP_001276718.1:p.Met532Arg
|
|
NM_001289790.1:c.1394T>G
|
NP_001276719.1:p.Met465Arg
|
|
XM_005258764.1:c.1478T>G
|
XP_005258821.1:p.Met493Arg
|
|
XM_006723148.1:c.1478T>G
|
XP_006723211.1:p.Met493Arg
|
|
XM_011526754.1:c.1595T>G
|
XP_011525056.1:p.Met532Arg
|
|
NM_000175.5:c.1478T>G
MANE Select
|
NP_000166.2:p.Met493Arg
|
|
NM_001289790.2:c.1394T>G
|
NP_001276719.1:p.Met465Arg
|
|
NM_001329909.1:c.1478T>G
|
NP_001316838.1:p.Met493Arg
|
|
NM_001329910.1:c.1478T>G
|
NP_001316839.1:p.Met493Arg
|
|
NM_001329911.1:c.1451T>G
|
NP_001316840.1:p.Met484Arg
|
|
XM_011526754.3:c.1595T>G
|
XP_011525056.1:p.Met532Arg
|
|
NM_001289790.3:c.1394T>G
|
NP_001276719.1:p.Met465Arg
|
|
NM_001329911.2:c.1451T>G
|
NP_001316840.1:p.Met484Arg
|
|