ENST00000236671.7:c.1118T>A
MANE Select
|
ENSP00000236671.2:p.Met373Lys
|
|
ENST00000367196.4:c.1013T>A
|
ENSP00000356164.4:p.Met338Lys
|
|
ENST00000427721.3:c.543T>A
|
|
|
ENST00000429746.2:c.1013T>A
|
ENSP00000402586.2:p.Met338Lys
|
|
ENST00000433655.6:c.*284T>A
|
ENSP00000404902.1:n.*284T>A
|
|
ENST00000438213.6:c.1235T>A
|
ENSP00000415036.2:p.Met412Lys
|
|
ENST00000636397.1:c.1071+179T>A
|
ENSP00000489910.1:n.1071+179T>A
|
|
ENST00000636571.1:c.1097T>A
|
ENSP00000490770.1:p.Met366Lys
|
|
ENST00000636579.1:c.72+179T>A
|
ENSP00000490489.1:n.72+179T>A
|
|
ENST00000636615.1:c.1071+179T>A
|
ENSP00000490014.1:n.1071+179T>A
|
|
ENST00000636843.1:c.1112T>A
|
ENSP00000490897.1:p.Met371Lys
|
|
ENST00000637158.1:n.716T>A
|
|
|
ENST00000637381.2:n.3546T>A
|
|
|
ENST00000637387.1:c.1097T>A
|
ENSP00000490598.1:p.Met366Lys
|
|
ENST00000637815.2:c.1100T>A
|
ENSP00000490344.1:p.Met367Lys
|
|
ENST00000637915.1:c.1109T>A
|
ENSP00000490471.1:p.Met370Lys
|
|
ENST00000637937.1:n.426T>A
|
|
|
ENST00000678991.1:c.*979T>A
|
ENSP00000503019.1:n.*979T>A
|
|
ENST00000236671.6:c.1118T>A
|
ENSP00000236671.2:p.Met373Lys
|
|
ENST00000427721.2:c.471+179T>A
|
ENSP00000415840.2:n.471+179T>A
|
|
ENST00000429746.1:c.449T>A
|
ENSP00000402586.1:p.Met150Lys
|
|
ENST00000433655.5:c.*284T>A
|
ENSP00000404902.1:n.*284T>A
|
|
NM_001909.4:c.1118T>A
|
NP_001900.1:p.Met373Lys
|
|
NM_001909.5:c.1118T>A
MANE Select
|
NP_001900.1:p.Met373Lys
|
|