|
ENST00000696138.1:c.7103T>C
|
ENSP00000512431.1:p.Met2368Thr
|
|
|
ENST00000684826.1:c.1685T>C
|
ENSP00000509994.1:p.Met562Thr
|
|
|
ENST00000687027.1:c.1277T>C
|
ENSP00000508715.1:p.Met426Thr
|
|
|
ENST00000687863.1:n.3766T>C
|
|
|
|
ENST00000689464.1:c.60T>C
|
|
|
|
ENST00000691014.1:c.7151T>C
|
ENSP00000510595.1:p.Met2384Thr
|
|
|
ENST00000693617.1:c.1685T>C
|
ENSP00000510031.1:p.Met562Thr
|
|
|
ENST00000358273.9:c.7121T>C
MANE Select
|
ENSP00000351015.4:p.Met2374Thr
|
|
|
ENST00000356175.7:c.7058T>C
|
ENSP00000348498.3:p.Met2353Thr
|
|
|
ENST00000358273.8:c.7121T>C
|
ENSP00000351015.4:p.Met2374Thr
|
|
|
ENST00000456735.6:c.6056T>C
|
ENSP00000389907.2:p.Met2019Thr
|
|
|
ENST00000471572.6:c.504T>C
|
|
|
|
ENST00000579081.5:c.7257T>C
|
ENSP00000462408.1:n.7257T>C
|
|
|
ENST00000581790.5:c.264T>C
|
|
|
|
ENST00000582892.1:n.363T>C
|
|
|
|
ENST00000584328.1:n.535T>C
|
|
|
|
NM_000267.3:c.7058T>C , LRG_214t1:c.7058T>C
|
NP_000258.1:p.Met2353Thr
|
|
|
NM_001042492.2:c.7121T>C , LRG_214t2:c.7121T>C
|
NP_001035957.1:p.Met2374Thr
|
|
|
XM_005257983.1:c.7121T>C
|
XP_005258040.1:p.Met2374Thr
|
|
|
XM_005257984.1:c.7058T>C
|
XP_005258041.1:p.Met2353Thr
|
|
|
XM_006721922.1:c.7151T>C
|
XP_006721985.1:p.Met2384Thr
|
|
|
XM_006721923.2:c.7112T>C
|
XP_006721986.1:p.Met2371Thr
|
|
|
XM_006721924.1:c.7151T>C
|
XP_006721987.1:p.Met2384Thr
|
|
|
XM_006721925.1:c.7088T>C
|
XP_006721988.1:p.Met2363Thr
|
|
|
XM_006721926.2:c.7151T>C
|
XP_006721989.1:p.Met2384Thr
|
|
|
XM_006721927.1:c.7151T>C
|
XP_006721990.1:p.Met2384Thr
|
|
|
XM_011524852.1:c.7148T>C
|
XP_011523154.1:p.Met2383Thr
|
|
|
XM_011524853.1:c.7112T>C
|
XP_011523155.1:p.Met2371Thr
|
|
|
XM_011524854.1:c.7112T>C
|
XP_011523156.1:p.Met2371Thr
|
|
|
XM_011524855.1:c.7112T>C
|
XP_011523157.1:p.Met2371Thr
|
|
|
XM_011524856.1:c.7112T>C
|
XP_011523158.1:p.Met2371Thr
|
|
|
XM_011524857.1:c.7151T>C
|
XP_011523159.1:p.Met2384Thr
|
|
|
NM_001042492.3:c.7121T>C
MANE Select
|
NP_001035957.1:p.Met2374Thr
|
|
